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nsv6141807

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:602,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1481 SVs from 95 studies. See in: genome view    
Submitted genomic72,698,779-73,300,779Question Mark
Overlapping variant regions from other studies: 756 SVs from 54 studies. See in: genome view    
Remapped(Score: Good):228,028-830,015Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6141807Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr772,698,77973,300,779
nsv6141807RemappedGoodGRCh37.p13PATCHESFirst PassNW_003871064.1Chr7|NW_00
3871064.1
228,028830,015

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16998028duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16998028Submitted genomicNC_000007.14:g.726
98779_73300779dup
GRCh38 (hg38)NC_000007.14Chr772,698,77973,300,779
nssv16998028RemappedGoodNW_003871064.1:g.2
28028_830015dup
GRCh37.p13First PassNW_003871064.1Chr7|NW_00
3871064.1
228,028830,015

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16998028<0.00166282
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