A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601090



Internal ID16388499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19840261..19859666hg38UCSC Ensembl
Innerchr6:19840492..19859897hg19UCSC Ensembl
Innerchr6:19948471..19967876hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3819406
hg1919406
hg1819406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1050877
Samples
Known GenesID4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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