A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696152



Internal ID15432804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157318026..157329832hg38UCSC Ensembl
Innerchr7:157110720..157122526hg19UCSC Ensembl
Innerchr7:156803481..156815287hg18UCSC Ensembl
Innerchr7:156610196..156622002hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3811807
hg1911807
hg1811807
hg1711807
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518702
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696152
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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