A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001679



Internal ID18744210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46767886..46804874hg38UCSC Ensembl
Innerchr3:46809376..46846364hg19UCSC Ensembl
Innerchr3:46784380..46821368hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3836989
hg1936989
hg1836989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3595200
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)nsv1001679
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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