A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068



Internal ID15550940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:7741876..7809624hg38UCSC Ensembl
Outerchr8:7599398..7667146hg19UCSC Ensembl
Outerchr8:7636808..7704556hg18UCSC Ensembl
Outerchr8:7636808..7704556hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3867749
hg1967749
hg1867749
hg1767749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10606, nssv9456
SamplesNA18956, NA18517
Known GenesFAM90A10P, PRR23D1, PRR23D2
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)nsv6068
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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