A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004089



Internal ID19093306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20348253..20450952hg38UCSC Ensembl
Innerchr3:20389745..20492444hg19UCSC Ensembl
Innerchr3:20364749..20467448hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38102700
hg19102700
hg18102700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593101
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)nsv1004089
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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