A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006002



Internal ID19095220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164304118..164935784hg38UCSC Ensembl
Innerchr3:164021906..164653572hg19UCSC Ensembl
Innerchr3:165504600..166136266hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38631667
hg19631667
hg18631667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614541
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)nsv1006002
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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