A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744066



Internal ID16038022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13527805..13529296hg38UCSC Ensembl
Innerchr10:13569805..13571296hg19UCSC Ensembl
Innerchr10:13609811..13611302hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381492
hg191492
hg181492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549990
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744066
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