A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768329



Internal ID15715599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17691960..17770275hg38UCSC Ensembl
Innerchr11:17713507..17791822hg19UCSC Ensembl
Innerchr11:17670083..17748398hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3878316
hg1978316
hg1878316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553588
Supporting Variants
Samples
Known GenesKCNC1, MYOD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768329
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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