A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150241



Internal ID15507681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:33840046..33917382hg38UCSC Ensembl
Innerchr18:31420010..31497346hg19UCSC Ensembl
Innerchr18:29674008..29751344hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3877337
hg1977337
hg1877337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576646
Supporting Variants
Samples1780862093_A
Known GenesNOL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150241
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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