A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764645



Internal ID16058601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4364953..4393643hg38UCSC Ensembl
Innerchr11:4386183..4414873hg19UCSC Ensembl
Innerchr11:4342759..4371449hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3828691
hg1928691
hg1828691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553156
Supporting Variants
Samples
Known GenesOR52B4, TRIM21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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