A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1050877



Internal ID15904063
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 StatusS
Merged Variantsnsv601090
Supporting Variants
Samples
Known GenesID4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1050877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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