A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549827



Internal ID15990550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3084883..3087280hg38UCSC Ensembl
Innerchr10:3127075..3129472hg19UCSC Ensembl
Innerchr10:3117075..3119472hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg382398
hg192398
hg182398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740406, nssv740415, nssv740410, nssv740414, nssv740413, nssv740417, nssv740418, nssv740411, nssv740409, nssv740407, nssv740405, nssv740412, nssv740408, nssv740416
Samples
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549827
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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