A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1295



Internal ID15197740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14900505..14974768hg38UCSC Ensembl
Outerchr16:14994362..15068625hg19UCSC Ensembl
Outerchr16:14901863..14976126hg18UCSC Ensembl
Outerchr16:14901863..14976126hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3874264
hg1974264
hg1874264
hg1774264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7277
Supporting Variants
SamplesNA19240
Known GenesLOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, 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)nssv1295
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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