A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702015



Internal ID15438667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84556843..84673561hg38UCSC Ensembl
Innerchr7:84186159..84302877hg19UCSC Ensembl
Innerchr7:84024095..84140813hg18UCSC Ensembl
Innerchr7:83830810..83947528hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38116719
hg19116719
hg18116719
hg17116719
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525826
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702015
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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