A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013676



Internal ID18756208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3627158..3718836hg38UCSC Ensembl
Innerchr3:3668842..3760520hg19UCSC Ensembl
Innerchr3:3643842..3735520hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3891679
hg1991679
hg1891679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590386
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)nsv1013676
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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