A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601302



Internal ID16042025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29890188..29901207hg38UCSC Ensembl
Innerchr6:29857965..29868984hg19UCSC Ensembl
Innerchr6:29965944..29976963hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3811020
hg1911020
hg1811020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10350n54
Supporting Variantsnssv1051865
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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