A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999883



Internal ID18812733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105968787..106288945hg38UCSC Ensembl
Innerchr3:105687634..106007792hg19UCSC Ensembl
Innerchr3:107170324..107490482hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38320159
hg19320159
hg18320159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604394
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)nsv999883
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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