A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174268



Internal ID15877671
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 StatusS
Merged Variantsnsv552228
Supporting Variants
SamplesHGDP01028
Known GenesMIR5694
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174268
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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