A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012343



Internal ID19101561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22519242..22769891hg38UCSC Ensembl
Innerchr3:22560733..22811382hg19UCSC Ensembl
Innerchr3:22535737..22786386hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38250650
hg19250650
hg18250650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589488
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)nsv1012343
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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