A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552192



Internal ID16339601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113443715..113457106hg38UCSC Ensembl
Innerchr10:115203474..115216865hg19UCSC Ensembl
Innerchr10:115193464..115206855hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3813392
hg1913392
hg1813392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1397n54
Supporting Variantsnssv758766
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552192
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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