A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011300



Internal ID18753834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46767886..46808087hg38UCSC Ensembl
Innerchr3:46809376..46849577hg19UCSC Ensembl
Innerchr3:46784380..46824581hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3840202
hg1940202
hg1840202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3595219, nssv3595216, nssv3595212, nssv3595208, nssv3595213, nssv3595223, nssv3595221, nssv3595217, nssv3595210, nssv3595215, nssv3595218, nssv3595209, nssv3595220, nssv3595214, nssv3595222, nssv3595224, nssv3595225, nssv3595211
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)nsv1011300
Frequency
Sample Size29084
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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