A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878076



Internal ID15825346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9913348..9914940hg38UCSC Ensembl
Innerchr18:9913345..9914937hg19UCSC Ensembl
Innerchr18:9903345..9904937hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381593
hg191593
hg181593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576455
Supporting Variants
Samples
Known GenesVAPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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