A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550715



Internal ID15991438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45383460..45402908hg38UCSC Ensembl
Innerchr10:45878908..45898356hg19UCSC Ensembl
Innerchr10:45198914..45218362hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3819449
hg1919449
hg1819449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173571
SamplesHGDP00869
Known GenesALOX5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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