A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156887



Internal ID15508428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140610939..140669718hg38UCSC Ensembl
Innerchr8:141621038..141679817hg19UCSC Ensembl
Innerchr8:141690220..141748999hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3858780
hg1958780
hg1858780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612569
Supporting Variants
Samples1780862444_A
Known GenesAGO2, PTK2, RNU6-31P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156887
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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