A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552191



Internal ID16339600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113443715..113455144hg38UCSC Ensembl
Innerchr10:115203474..115214903hg19UCSC Ensembl
Innerchr10:115193464..115204893hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3811430
hg1911430
hg1811430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1397n54
Supporting Variantsnssv758765
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552191
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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