A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5665



Internal ID15197081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:59999780..60108294hg38UCSC Ensembl
Outerchr17:58077141..58185655hg19UCSC Ensembl
Outerchr17:55431923..55540437hg18UCSC Ensembl
Outerchr17:55431923..55540437hg17UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38108515
hg19108515
hg18108515
hg17108515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7295
Supporting Variants
SamplesNA19129
Known GenesHEATR6, LOC645638, LOC653653, MIR4737, TBC1D3P1-DHX40P1
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)nssv5665
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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