A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174988



Internal ID15873078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64344602..64477466hg38UCSC Ensembl
Innerchr10:66104362..66237223hg19UCSC Ensembl
Innerchr10:65774368..65907229hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38132865
hg19132862
hg18132862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551201
Supporting Variants
SamplesHGDP00113
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174988
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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