A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553750



Internal ID16341159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22998359..23022607hg38UCSC Ensembl
Innerchr11:23019905..23044153hg19UCSC Ensembl
Innerchr11:22976481..23000729hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3824249
hg1924249
hg1824249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1693n54
Supporting Variantsnssv768948, nssv768949
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553750
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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