A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5666



Internal ID15197080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:60034691..60151634hg38UCSC Ensembl
Outerchr17:58112052..58228995hg19UCSC Ensembl
Outerchr17:55466834..55583777hg18UCSC Ensembl
Outerchr17:55466834..55583777hg17UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38116944
hg19116944
hg18116944
hg17116944
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7295
Supporting Variants
SamplesNA19129
Known GenesCA4, HEATR6, LOC645638, LOC653653, MIR4737
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)nssv5666
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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