A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10131



Internal ID15195981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:68843987..68878871hg38UCSC Ensembl
Outerchr17:66840128..66875012hg19UCSC Ensembl
Outerchr17:64351723..64386607hg18UCSC Ensembl
Outerchr17:64351723..64386607hg17UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3834885
hg1934885
hg1834885
hg1734885
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7296
Supporting Variants
SamplesNA18956
Known GenesABCA8
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)nssv10131
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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