A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10947



Internal ID15192849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14902607..15000623hg38UCSC Ensembl
Outerchr16:14996464..15094480hg19UCSC Ensembl
Outerchr16:14903965..15001981hg18UCSC Ensembl
Outerchr16:14903965..15001981hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3898017
hg1998017
hg1898017
hg1798017
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7277
Supporting Variants
SamplesNA15510
Known GenesLOC100288162, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, 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)nssv10947
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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