A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694733



Internal ID15431385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:36406247..36414652hg38UCSC Ensembl
Innerchr7:36445856..36454261hg19UCSC Ensembl
Innerchr7:36412381..36420786hg18UCSC Ensembl
Innerchr7:36219096..36227501hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg388406
hg198406
hg188406
hg178406
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521965
Supporting Variants
Samples
Known GenesANLN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694733
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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