A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550016



Internal ID15990739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15334858..15477923hg38UCSC Ensembl
Innerchr10:15376857..15519922hg19UCSC Ensembl
Innerchr10:15416863..15559928hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38143066
hg19143066
hg18143066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174134
SamplesHGDP00423
Known GenesFAM171A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550016
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