A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660096



Internal ID15396748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45653..93811hg38UCSC Ensembl
Innerchr7:45653..93811hg19UCSC Ensembl
Innerchr7:140736..188894hg18UCSC Ensembl
Innerchr7:140736..188894hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3848159
hg1948159
hg1848159
hg1748159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516015
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660096
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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