A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174092



Internal ID15529575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:209282..520255hg38UCSC Ensembl
Innerchr10:255222..566195hg19UCSC Ensembl
Innerchr10:245222..556195hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38310974
hg19310974
hg18310974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549750
Supporting Variants
SamplesHGDP00811
Known GenesDIP2C, ZMYND11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174092
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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