A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552322



Internal ID16339731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130385100..131017580hg38UCSC Ensembl
Innerchr10:132183364..132815843hg19UCSC Ensembl
Innerchr10:132073354..132705833hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38632481
hg19632480
hg18632480
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760803
Samples
Known GenesMIR378C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552322
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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