A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10078



Internal ID15196033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14725681..15327108hg38UCSC Ensembl
Outerchr16:14819538..15420965hg19UCSC Ensembl
Outerchr16:14727039..15328466hg18UCSC Ensembl
Outerchr16:14727039..15328466hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38601428
hg19601428
hg18601428
hg17601428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7277
Supporting Variants
SamplesNA18956
Known GenesABCC6P2, LOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR3180-4, MIR6511A-2, MIR6511B-1, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, NTAN1, PDXDC1, RRN3
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)nssv10078
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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