A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552294



Internal ID16339703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126262640..126274525hg38UCSC Ensembl
Innerchr10:127951209..127963094hg19UCSC Ensembl
Innerchr10:127941199..127953084hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3811886
hg1911886
hg1811886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174580
SamplesHGDP00748
Known GenesADAM12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552294
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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