A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031737



Internal ID18774271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144830982..144986209hg38UCSC Ensembl
Innerchr8:146056367..146211595hg19UCSC Ensembl
Innerchr8:146027171..146182399hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38155228
hg19155229
hg18155229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690120
Samples
Known GenesCOMMD5, ZNF16, ZNF250, ZNF252P, ZNF7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031737
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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