A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10084



Internal ID15196027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:16633136..18760373hg38UCSC Ensembl
Outerchr16:16726993..18771695hg19UCSC Ensembl
Outerchr16:16634494..18679196hg18UCSC Ensembl
Outerchr16:16634494..18679196hg17UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg382127238
hg192044703
hg182044703
hg172044703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7278
Supporting Variants
SamplesNA18956
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8, XYLT1
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)nssv10084
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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