A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9767



Internal ID15540091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70699414..70741309hg38UCSC Ensembl
Outerchr9:73314330..73356225hg19UCSC Ensembl
Outerchr9:72504150..72546045hg18UCSC Ensembl
Outerchr9:70543884..70585779hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3841896
hg1941896
hg1841896
hg1741896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6556
Supporting Variants
SamplesNA18507
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)nssv9767
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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