A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366



Internal ID15204582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:120511588..120518414hg38UCSC Ensembl
Outerchr8:121523828..121530654hg19UCSC Ensembl
Outerchr8:121593009..121599835hg18UCSC Ensembl
Outerchr8:121593009..121599835hg17UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg386827
hg196827
hg186827
hg176827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8547
SamplesNA12156
Known GenesMTBP
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)nsv6366
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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