A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665140



Internal ID15401792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:49313068..49386210hg38UCSC Ensembl
Innerchr7:49352664..49425806hg19UCSC Ensembl
Innerchr7:49323210..49396352hg18UCSC Ensembl
Innerchr7:49129925..49203067hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3873143
hg1973143
hg1873143
hg1773143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515884
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665140
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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