A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878046



Internal ID16172002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8705253..8706431hg38UCSC Ensembl
Innerchr18:8705251..8706429hg19UCSC Ensembl
Innerchr18:8695251..8696429hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381179
hg191179
hg181179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576438
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878046
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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