A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549805



Internal ID15990528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2661867..3082324hg38UCSC Ensembl
Innerchr10:2704059..3124516hg19UCSC Ensembl
Innerchr10:2694059..3114516hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38420458
hg19420458
hg18420458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv933n54
Supporting Variantsnssv740237
Samples
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549805
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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