A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549828



Internal ID15990551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3084883..3091456hg38UCSC Ensembl
Innerchr10:3127075..3133648hg19UCSC Ensembl
Innerchr10:3117075..3123648hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg386574
hg196574
hg186574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv939n54
Supporting Variantsnssv740419, nssv740432, nssv740430, nssv740428, nssv740422, nssv740425, nssv740420, nssv740423, nssv740424, nssv740427, nssv740426, nssv740421, nssv740431, nssv740429
Samples
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549828
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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