A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553772



Internal ID16341181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23980429..24039539hg38UCSC Ensembl
Innerchr11:24001975..24061085hg19UCSC Ensembl
Innerchr11:23958551..24017661hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3859111
hg1959111
hg1859111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174753
Samples1780854481_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553772
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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