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dbVar

Database of genomic structural variation

nsv4393350

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:268,796

Links to Other Resources

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: 1001 SVs from 72 studies. See in: genome view

Remapped(Score: Perfect):99,569,388-99,838,183

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
nsv4393350	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	99,569,388	99,576,420	99,831,116	99,838,183
nsv4393350	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	98,905,092	98,912,124	99,166,820	99,173,887

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15711948	copy number gain	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15711948	Remapped	Perfect	NC_000005.10:g.(99 569388_99576420)_( 99831116_99838183) dup	GRCh38.p12	First Pass	NC_000005.10	Chr5	99,569,388	99,576,420	99,831,116	99,838,183
nssv15711948	Submitted genomic		NC_000005.9:g.(989 05092_98912124)_(9 9166820_99173887)d up	GRCh37 (hg19)		NC_000005.9	Chr5	98,905,092	98,912,124	99,166,820	99,173,887

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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