A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552277



Internal ID16339686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124233394..124303903hg38UCSC Ensembl
Innerchr10:125921963..125992472hg19UCSC Ensembl
Innerchr10:125911953..125982462hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3870510
hg1970510
hg1870510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760475
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552277
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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