A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878032



Internal ID15825302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8705082..8706529hg38UCSC Ensembl
Innerchr18:8705080..8706527hg19UCSC Ensembl
Innerchr18:8695080..8696527hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381448
hg191448
hg181448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576433
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)nssv878032
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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