A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552291



Internal ID16339700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125362698..125398525hg38UCSC Ensembl
Innerchr10:127051267..127087094hg19UCSC Ensembl
Innerchr10:127041257..127077084hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3835828
hg1935828
hg1835828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1416n54
Supporting Variantsnssv1174578
SamplesHGDP00743
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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