A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1076649



Internal ID15929835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166783908..166784539hg38UCSC Ensembl
Innerchr6:167197396..167198027hg19UCSC Ensembl
Innerchr6:167117386..167118017hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38632
hg19632
hg18632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605329
Supporting Variants
Samples
Known GenesRPS6KA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1076649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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