A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601948



Internal ID16042671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31817661..31827186hg38UCSC Ensembl
Innerchr6:31785438..31794963hg19UCSC Ensembl
Innerchr6:31893417..31902942hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg389526
hg199526
hg189526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10462n54
Supporting Variantsnssv1053530, nssv1053529
Samples
Known GenesHSPA1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601948
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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