A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999085



Internal ID19158621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22043027..22139678hg38UCSC Ensembl
Innerchr3:22084519..22181170hg19UCSC Ensembl
Innerchr3:22059523..22156174hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3896652
hg1996652
hg1896652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739650
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)nsv999085
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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