A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155944



Internal ID15507989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1733567..1805331hg38UCSC Ensembl
Innerchr8:1681733..1753497hg19UCSC Ensembl
Innerchr8:1669140..1740904hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3871765
hg1971765
hg1871765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609527
Supporting Variants
Samples1780862275_A
Known GenesCLN8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155944
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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