A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006921



Internal ID19096139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:23080476..23113674hg38UCSC Ensembl
Innerchr3:23121967..23155165hg19UCSC Ensembl
Innerchr3:23096971..23130169hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3833199
hg1933199
hg1833199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4701n100
Supporting Variantsnssv3589493
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)nsv1006921
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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