A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012523



Internal ID18755056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:66692572..66734240hg38UCSC Ensembl
Innerchr2:66919704..66961372hg19UCSC Ensembl
Innerchr2:66773208..66814876hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3841669
hg1941669
hg1841669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577275
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)nsv1012523
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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