A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552754



Internal ID16340163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133761946..133774701hg38UCSC Ensembl
Innerchr10:135499271..135512026hg19UCSC Ensembl
Innerchr10:135349261..135362016hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3812756
hg1912756
hg1812756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1503n54
Supporting Variantsnssv763029
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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