A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005213



Internal ID19094430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32499518..32650274hg38UCSC Ensembl
Innerchr1:32965119..33115875hg19UCSC Ensembl
Innerchr1:32737706..32888462hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38150757
hg19150757
hg18150757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3472615
Samples
Known GenesZBTB8A, ZBTB8OS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005213
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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