A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700692



Internal ID15437344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89907951..89908793hg38UCSC Ensembl
Innerchr7:89537265..89538107hg19UCSC Ensembl
Innerchr7:89375201..89376043hg18UCSC Ensembl
Innerchr7:89181916..89182758hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38843
hg19843
hg18843
hg17843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515997
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700692
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer