A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1061124



Internal ID15914310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61744448..61941158hg38UCSC Ensembl
Innerchr6:62454353..62651063hg19UCSC Ensembl
Innerchr6:62512312..62709022hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38196711
hg19196711
hg18196711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603315
Supporting Variants
Samples
Known GenesKHDRBS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1061124
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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