A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998319



Internal ID18811169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21957988..21991872hg38UCSC Ensembl
Innerchr3:21999480..22033364hg19UCSC Ensembl
Innerchr3:21974484..22008368hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3833885
hg1933885
hg1833885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589475
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)nsv998319
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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