A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551940



Internal ID16339349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92908767..92965751hg38UCSC Ensembl
Innerchr10:94668524..94725508hg19UCSC Ensembl
Innerchr10:94658504..94715488hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3856985
hg1956985
hg1856985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174727
SamplesHGDP00150
Known GenesEXOC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551940
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