A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689083



Internal ID15425735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45653..112828hg38UCSC Ensembl
Innerchr7:45653..112828hg19UCSC Ensembl
Innerchr7:140736..207911hg18UCSC Ensembl
Innerchr7:140736..207911hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3867176
hg1967176
hg1867176
hg1767176
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)nssv689083
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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