A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv882627



Internal ID16176583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44398116..44404983hg38UCSC Ensembl
Innerchr18:41978081..41984948hg19UCSC Ensembl
Innerchr18:40232079..40238946hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg386868
hg196868
hg186868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576801
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)nssv882627
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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