A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553090



Internal ID15993813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2394970..2402590hg38UCSC Ensembl
Innerchr11:2416200..2423820hg19UCSC Ensembl
Innerchr11:2372776..2380396hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387621
hg197621
hg187621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1569n54
Supporting Variantsnssv764512
Samples
Known GenesCD81, TSSC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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