A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698074



Internal ID15434726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97759718..97771587hg38UCSC Ensembl
Innerchr7:97389030..97400899hg19UCSC Ensembl
Innerchr7:97226966..97238835hg18UCSC Ensembl
Innerchr7:97033681..97045550hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811870
hg1911870
hg1811870
hg1711870
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516307
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698074
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