A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878365



Internal ID16172321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11917411..11986558hg38UCSC Ensembl
Innerchr18:11917410..11986557hg19UCSC Ensembl
Innerchr18:11907410..11976557hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3869148
hg1969148
hg1869148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576495
Supporting Variants
Samples
Known GenesIMPA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878365
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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