A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013613



Internal ID18756145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:63318463..63379554hg38UCSC Ensembl
Innerchr2:63545598..63606689hg19UCSC Ensembl
Innerchr2:63399102..63460193hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3861092
hg1961092
hg1861092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3860n100
Supporting Variantsnssv3577257
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)nsv1013613
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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