A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1050624



Internal ID15903810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18980521..19030499hg38UCSC Ensembl
Innerchr6:18980752..19030730hg19UCSC Ensembl
Innerchr6:19088731..19138709hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3849979
hg1949979
hg1849979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601060
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1050624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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