A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003419



Internal ID19092637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26549785..26579428hg38UCSC Ensembl
Innerchr3:26591276..26620919hg19UCSC Ensembl
Innerchr3:26566280..26595923hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3829644
hg1929644
hg1829644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589560
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)nsv1003419
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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