A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551527



Internal ID15992250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73949148..74140704hg38UCSC Ensembl
Innerchr10:75708906..75900462hg19UCSC Ensembl
Innerchr10:75378912..75570468hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38191557
hg19191557
hg18191557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750286
Samples
Known GenesAP3M1, VCL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551527
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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