A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878958



Internal ID15826228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:33858846..33866413hg38UCSC Ensembl
Innerchr18:31438810..31446377hg19UCSC Ensembl
Innerchr18:29692808..29700375hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg387568
hg197568
hg187568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576647
Supporting Variants
Samples
Known GenesNOL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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