A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv916091



Internal ID16210047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:112288077..112290856hg38UCSC Ensembl
Innerchr2:113045654..113048433hg19UCSC Ensembl
Innerchr2:112762125..112764904hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg382780
hg192780
hg182780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582705
Supporting Variants
Samples
Known GenesZC3H6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv916091
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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