A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012628



Internal ID18755160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:63318463..63377724hg38UCSC Ensembl
Innerchr2:63545598..63604859hg19UCSC Ensembl
Innerchr2:63399102..63458363hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3859262
hg1959262
hg1859262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3860n100
Supporting Variantsnssv3577256
Samples
Known GenesWDPCP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012628
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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