A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550225



Internal ID16337634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25364088..25382453hg38UCSC Ensembl
Innerchr10:25653017..25671382hg19UCSC Ensembl
Innerchr10:25693023..25711388hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818366
hg1918366
hg1818366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744737, nssv744736
Samples
Known GenesGPR158
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550225
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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