A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748927



Internal ID15696197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63501424..63719655hg38UCSC Ensembl
Innerchr10:65261184..65479415hg19UCSC Ensembl
Innerchr10:64931190..65149421hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38218232
hg19218232
hg18218232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551184
Supporting Variants
Samples
Known GenesREEP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv748927
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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