A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6198



Internal ID15551083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:55202492..55247765hg38UCSC Ensembl
Outerchr8:56115052..56160325hg19UCSC Ensembl
Outerchr8:56277606..56322879hg18UCSC Ensembl
Outerchr8:56277606..56322879hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3845274
hg1945274
hg1845274
hg1745274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8493
SamplesNA12156
Known GenesXKR4
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)nsv6198
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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