A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999644



Internal ID18812494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62687068..62712793hg38UCSC Ensembl
Innerchr3:62672743..62698468hg19UCSC Ensembl
Innerchr3:62647783..62673508hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3825726
hg1925726
hg1825726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4756n100
Supporting Variantsnssv3594573
Samples
Known GenesCADPS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999644
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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