A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174277



Internal ID15875998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1616814..1629034hg38UCSC Ensembl
Innerchr11:1638044..1650264hg19UCSC Ensembl
Innerchr11:1594620..1606840hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3812221
hg1912221
hg1812221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553001
Supporting Variants
SamplesHGDP00771
Known GenesKRTAP5-4, MOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174277
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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