A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744715



Internal ID15691985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:23193706..23334594hg38UCSC Ensembl
Innerchr10:23482635..23623523hg19UCSC Ensembl
Innerchr10:23522641..23663529hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38140889
hg19140889
hg18140889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550213
Supporting Variants
Samples
Known GenesC10orf115, C10orf67, PTF1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744715
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