A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555604



Internal ID16343013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83085381..83125337hg38UCSC Ensembl
Innerchr11:82796423..82836379hg19UCSC Ensembl
Innerchr11:82474071..82514027hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3839957
hg1939957
hg1839957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779846, nssv1176183
SamplesNINDS_236
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555604
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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