A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878957



Internal ID15826227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:33671257..34001283hg38UCSC Ensembl
Innerchr18:31251221..31581247hg19UCSC Ensembl
Innerchr18:29505219..29835245hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38330027
hg19330027
hg18330027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576643
Supporting Variants
Samples
Known GenesASXL3, NOL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878957
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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