A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174639



Internal ID15881274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40246547..40276760hg38UCSC Ensembl
Innerchr11:40268097..40298310hg19UCSC Ensembl
Innerchr11:40224673..40254886hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3830214
hg1930214
hg1830214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554086
Supporting Variants
SamplesNINDS_94
Known GenesLRRC4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174639
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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