A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154026



Internal ID15879906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19776428..19812213hg38UCSC Ensembl
Innerchr6:19776659..19812444hg19UCSC Ensembl
Innerchr6:19884638..19920423hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3835786
hg1935786
hg1835786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601088
Supporting Variants
SamplesNINDS_125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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