A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151115



Internal ID15855426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:100071316..100137028hg38UCSC Ensembl
Innerchr2:100687778..100753490hg19UCSC Ensembl
Innerchr2:100054210..100119922hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3865713
hg1965713
hg1865713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582529
Supporting Variants
Samples1780862592_A
Known GenesAFF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151115
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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