A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008120



Internal ID18750651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46767886..46806114hg38UCSC Ensembl
Innerchr3:46809376..46847604hg19UCSC Ensembl
Innerchr3:46784380..46822608hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3838229
hg1938229
hg1838229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3595203, nssv3595202, nssv3595201, nssv3595204
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)nsv1008120
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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