A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006731



Internal ID19095949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66210220..66251828hg38UCSC Ensembl
Innerchr4:67075938..67117546hg19UCSC Ensembl
Innerchr4:66758533..66800141hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3841609
hg1941609
hg1841609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3740195
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)nsv1006731
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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