A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998653



Internal ID18811503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46763621..46807677hg38UCSC Ensembl
Innerchr3:46805111..46849167hg19UCSC Ensembl
Innerchr3:46780115..46824171hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3844057
hg1944057
hg1844057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3595196
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)nsv998653
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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