A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696962



Internal ID15433614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148892777..148945913hg38UCSC Ensembl
Innerchr7:148589869..148643005hg19UCSC Ensembl
Innerchr7:148220802..148273938hg18UCSC Ensembl
Innerchr7:148027517..148080653hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3853137
hg1953137
hg1853137
hg1753137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519634
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696962
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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