A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552228



Internal ID16339637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121010375..121025489hg38UCSC Ensembl
Innerchr10:122769888..122785002hg19UCSC Ensembl
Innerchr10:122759878..122774992hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3815115
hg1915115
hg1815115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1405n54
Supporting Variantsnssv760292, nssv760283, nssv1174269, nssv1174267, nssv1174270, nssv760286, nssv1174268, nssv760288, nssv760293, nssv760291, nssv760285, nssv760287, nssv760289, nssv760294, nssv760290, nssv760282, nssv760281, nssv760284
SamplesHGDP01028, HGDP01408, HGDP01405, HGDP00620
Known GenesMIR5694
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552228
Frequency
Sample Size17421
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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