A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135266



Internal ID19281394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:67815084..67815414hg38UCSC Ensembl
Outerchr8:68727319..68727649hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3837n106
Supporting Variantsnssv3988823
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135266
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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