A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601315



Internal ID16042038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29918599hg38UCSC Ensembl
Innerchr6:29859517..29886376hg19UCSC Ensembl
Innerchr6:29967496..29994355hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3826860
hg1926860
hg1826860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10346n54
Supporting Variantsnssv1051930
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601315
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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