A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601173



Internal ID16041896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26239176..26322296hg38UCSC Ensembl
Innerchr6:26239404..26322524hg19UCSC Ensembl
Innerchr6:26347383..26430503hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3883121
hg1983121
hg1883121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051367
Samples
Known GenesHIST1H2BH, HIST1H2BI, HIST1H3F, HIST1H3G, HIST1H4F, HIST1H4G, HIST1H4H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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