A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9471



Internal ID15540185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70701587..70740661hg38UCSC Ensembl
Outerchr9:73316503..73355577hg19UCSC Ensembl
Outerchr9:72506323..72545397hg18UCSC Ensembl
Outerchr9:70546057..70585131hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3839075
hg1939075
hg1839075
hg1739075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556
Supporting Variants
SamplesNA18517
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)nssv9471
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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