A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455



Internal ID15551366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:918351..954194hg38UCSC Ensembl
Outerchr9:918351..954194hg19UCSC Ensembl
Outerchr9:908351..944194hg18UCSC Ensembl
Outerchr9:908351..944194hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3835844
hg1935844
hg1835844
hg1735844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8576
SamplesNA12156
Known GenesDMRT1
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)nsv6455
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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