A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1052391



Internal ID15905577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31301571..31346466hg38UCSC Ensembl
Innerchr6:31269348..31314243hg19UCSC Ensembl
Innerchr6:31377327..31422222hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3844896
hg1944896
hg1844896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601519
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1052391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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