A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10945



Internal ID15192847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14896933..14973551hg38UCSC Ensembl
Outerchr16:14990790..15067408hg19UCSC Ensembl
Outerchr16:14898291..14974909hg18UCSC Ensembl
Outerchr16:14898291..14974909hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3876619
hg1976619
hg1876619
hg1776619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7277
Supporting Variants
SamplesNA15510
Known GenesLOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NPIPA1
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)nssv10945
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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