A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv808



Internal ID15544669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70701687..70738551hg38UCSC Ensembl
Outerchr9:73316603..73353467hg19UCSC Ensembl
Outerchr9:72506423..72543287hg18UCSC Ensembl
Outerchr9:70546157..70583021hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3836865
hg1936865
hg1836865
hg1736865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556
Supporting Variants
SamplesNA19240
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)nssv808
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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