A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150250



Internal ID15876568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48637601..48664350hg38UCSC Ensembl
Innerchr18:46163972..46190721hg19UCSC Ensembl
Innerchr18:44417970..44444719hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3826750
hg1926750
hg1826750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576856
Supporting Variants
SamplesHGDP00862
Known GenesCTIF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150250
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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