A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601057



Internal ID16388466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18842328..18894005hg38UCSC Ensembl
Innerchr6:18842559..18894236hg19UCSC Ensembl
Innerchr6:18950538..19002215hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3851678
hg1951678
hg1851678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154187
SamplesNINDS_91
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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