A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549829



Internal ID15990552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3084883..3092489hg38UCSC Ensembl
Innerchr10:3127075..3134681hg19UCSC Ensembl
Innerchr10:3117075..3124681hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg387607
hg197607
hg187607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv939n54
Supporting Variantsnssv740433, nssv740434
Samples
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549829
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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