A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612229



Internal ID16399638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129200957..129239983hg38UCSC Ensembl
Innerchr8:130213203..130252229hg19UCSC Ensembl
Innerchr8:130282385..130321411hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3839027
hg1939027
hg1839027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1121155
Samples
Known GenesLINC00977
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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