A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552504



Internal ID15993227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132180474..132255847hg38UCSC Ensembl
Innerchr10:133993978..134069351hg19UCSC Ensembl
Innerchr10:133843968..133919341hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3875374
hg1975374
hg1875374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv761927
Samples
Known GenesDPYSL4, JAKMIP3, STK32C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552504
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer