A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768330



Internal ID15715600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17723445..17788177hg38UCSC Ensembl
Innerchr11:17744992..17809724hg19UCSC Ensembl
Innerchr11:17701568..17766300hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3864733
hg1964733
hg1864733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553589
Supporting Variants
Samples
Known GenesKCNC1, SERGEF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768330
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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