A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv882606



Internal ID16176562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44398116..44401251hg38UCSC Ensembl
Innerchr18:41978081..41981216hg19UCSC Ensembl
Innerchr18:40232079..40235214hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg383136
hg193136
hg183136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576798
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)nssv882606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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