A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552519



Internal ID16339928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132481908..132506606hg38UCSC Ensembl
Innerchr10:134295412..134320110hg19UCSC Ensembl
Innerchr10:134145402..134170100hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3824699
hg1924699
hg1824699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv761956
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552519
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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