A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486



Internal ID15551400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:15805222..15837641hg38UCSC Ensembl
Outerchr9:15805220..15837639hg19UCSC Ensembl
Outerchr9:15795220..15827639hg18UCSC Ensembl
Outerchr9:15795220..15827639hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3832420
hg1932420
hg1832420
hg1732420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv792, nssv3706
SamplesNA12878, NA19240
Known GenesCCDC171
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)nsv6486
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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