A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv761955



Internal ID16055911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132423184..132492159hg38UCSC Ensembl
Innerchr10:134236688..134305663hg19UCSC Ensembl
Innerchr10:134086678..134155653hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3868976
hg1968976
hg1868976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552518
Supporting Variants
Samples
Known GenesC10orf91
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv761955
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