A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032009



Internal ID19121231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166233661..166482083hg38UCSC Ensembl
Innerchr4:167154813..167403235hg19UCSC Ensembl
Innerchr4:167374263..167622685hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38248423
hg19248423
hg18248423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634171
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)nsv1032009
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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