A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553677



Internal ID16341086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19430237..19449896hg38UCSC Ensembl
Innerchr11:19451784..19471443hg19UCSC Ensembl
Innerchr11:19408360..19428019hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3819660
hg1919660
hg1819660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768700
Samples
Known GenesNAV2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553677
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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