A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551497



Internal ID16338906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70961606..70983197hg38UCSC Ensembl
Innerchr10:72721363..72742954hg19UCSC Ensembl
Innerchr10:72391369..72412960hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3821592
hg1921592
hg1821592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1262n54
Supporting Variantsnssv750259
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551497
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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