A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010067



Internal ID19099286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63255703..63424843hg38UCSC Ensembl
Innerchr4:64121421..64290561hg19UCSC Ensembl
Innerchr4:63804016..63973156hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38169141
hg19169141
hg18169141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5225n100
Supporting Variantsnssv3626534, nssv3626535, nssv3626536
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)nsv1010067
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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