A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174098



Internal ID15528391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2644284..3091456hg38UCSC Ensembl
Innerchr10:2686476..3133648hg19UCSC Ensembl
Innerchr10:2676476..3123648hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38447173
hg19447173
hg18447173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549803
Supporting Variants
SamplesHGDP00632
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174098
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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