A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558



Internal ID15551479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70974175..70985459hg38UCSC Ensembl
Outerchr9:73589091..73600375hg19UCSC Ensembl
Outerchr9:72778911..72790195hg18UCSC Ensembl
Outerchr9:70818645..70829929hg17UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3811285
hg1911285
hg1811285
hg1711285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8609
SamplesNA12156
Known GenesTRPM3
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)nsv6558
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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