A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474



Internal ID15551387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:8706602..8751414hg38UCSC Ensembl
Outerchr9:8706602..8751414hg19UCSC Ensembl
Outerchr9:8696602..8741414hg18UCSC Ensembl
Outerchr9:8696602..8741414hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3844813
hg1944813
hg1844813
hg1744813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8584
SamplesNA12156
Known GenesPTPRD
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)nsv6474
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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