A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997411



Internal ID19156947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41145482..41338480hg38UCSC Ensembl
Innerchr2:41372622..41565620hg19UCSC Ensembl
Innerchr2:41226126..41419124hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38192999
hg19192999
hg18192999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581557
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997411
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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