A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699064



Internal ID15089030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25561860..25566500hg38UCSC Ensembl
Innerchr7:25601480..25606120hg19UCSC Ensembl
Innerchr7:25568005..25572645hg18UCSC Ensembl
Innerchr7:25374720..25379360hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg384641
hg194641
hg184641
hg174641
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523322
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699064
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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