A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033429



Internal ID19122651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8881514..9023654hg38UCSC Ensembl
Innerchr7:8921144..9063284hg19UCSC Ensembl
Innerchr7:8887669..9029809hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38142141
hg19142141
hg18142141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6258n100
Supporting Variantsnssv3642858
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)nsv1033429
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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