A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549969



Internal ID16337378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12058736..12117648hg38UCSC Ensembl
Innerchr10:12100735..12159647hg19UCSC Ensembl
Innerchr10:12140741..12199653hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3858913
hg1958913
hg1858913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv956n54
Supporting Variantsnssv1174120
SamplesHGDP00908
Known GenesDHTKD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549969
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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