A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004128



Internal ID18746659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46828447hg38UCSC Ensembl
Innerchr3:46801805..46869937hg19UCSC Ensembl
Innerchr3:46776809..46844941hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3868133
hg1968133
hg1868133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4732n100
Supporting Variantsnssv3593767, nssv3593768
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)nsv1004128
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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