A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552295



Internal ID16339704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126682920..126880976hg38UCSC Ensembl
Innerchr10:128371489..128569545hg19UCSC Ensembl
Innerchr10:128361479..128559535hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38198057
hg19198057
hg18198057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1417n54
Supporting Variantsnssv760495
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552295
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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