A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344



Internal ID15551244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:107655965..107686182hg38UCSC Ensembl
Outerchr8:108668193..108698410hg19UCSC Ensembl
Outerchr8:108737369..108767586hg18UCSC Ensembl
Outerchr8:108737369..108767586hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg389293
hg199293
hg189293
hg179293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10637
SamplesNA18956
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6344
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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