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dbVar

Database of genomic structural variation

esv9725

Organism: Homo sapiens

Study:estd19 (Ahn et al. 2009)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:6,920

Publication(s):Ahn et al. 2009

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 314 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):20,933,069-20,939,988

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
esv9725	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	20,933,069	20,933,105	20,939,445	20,939,988
esv9725	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	18,513,030	18,513,066	18,519,406	18,519,949
esv9725	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000018.8	Chr18	16,767,028	16,767,064	16,773,404	16,773,947

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv32166	inversion	Sequencing	Read depth and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
essv32166	Remapped	Perfect	NC_000018.10:g.(20 933069_20933105)_( 20939445_20939988) inv	GRCh38.p12	First Pass	NC_000018.10	Chr18	20,933,069	20,933,105	20,939,445	20,939,988
essv32166	Remapped	Perfect	NC_000018.9:g.(185 13030_18513066)_(1 8519406_18519949)i nv	GRCh37.p13	First Pass	NC_000018.9	Chr18	18,513,030	18,513,066	18,519,406	18,519,949
essv32166	Submitted genomic		NC_000018.8:g.(167 67028_16767064)_(1 6773404_16773947)i nv	NCBI36 (hg18)		NC_000018.8	Chr18	16,767,028	16,767,064	16,773,404	16,773,947

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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