A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610778



Internal ID16051501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23316078..23341917hg38UCSC Ensembl
Innerchr8:23173591..23199430hg19UCSC Ensembl
Innerchr8:23229536..23255375hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3825840
hg1925840
hg1825840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107482
Samples
Known GenesLOC100507156, LOXL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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