A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601970



Internal ID16389379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31970674..31980252hg38UCSC Ensembl
Innerchr6:31938451..31948029hg19UCSC Ensembl
Innerchr6:32046430..32056008hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg389579
hg199579
hg189579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053564
Samples
Known GenesDXO, STK19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601970
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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