A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697571



Internal ID15434223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76794802..76853165hg38UCSC Ensembl
Innerchr2:77021928..77080291hg19UCSC Ensembl
Innerchr2:76875436..76933799hg18UCSC Ensembl
Innerchr2:76933583..76991946hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3858364
hg1958364
hg1858364
hg1758364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520715
Supporting Variants
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697571
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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