A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10080



Internal ID15196031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14881701..15024424hg38UCSC Ensembl
Outerchr16:14975558..15118281hg19UCSC Ensembl
Outerchr16:14883059..15025782hg18UCSC Ensembl
Outerchr16:14883059..15025782hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38142724
hg19142724
hg18142724
hg17142724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7277
Supporting Variants
SamplesNA18956
Known GenesLOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, PDXDC1
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)nssv10080
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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