A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150251



Internal ID15877815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48658158..48674681hg38UCSC Ensembl
Innerchr18:46184529..46201052hg19UCSC Ensembl
Innerchr18:44438527..44455050hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3816524
hg1916524
hg1816524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576857
Supporting Variants
SamplesHGDP01048
Known GenesCTIF, MIR4743
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150251
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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