A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703725



Internal ID15440377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56612139..56638484hg38UCSC Ensembl
Innerchr7:56679832..56706177hg19UCSC Ensembl
Innerchr7:56647326..56673671hg18UCSC Ensembl
Innerchr7:56454041..56480386hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3826346
hg1926346
hg1826346
hg1726346
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527305
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703725
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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