A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7277



Internal ID15205584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14725681..15360160hg38UCSC Ensembl
Outerchr16:14819538..15454017hg19UCSC Ensembl
Outerchr16:14727039..15361518hg18UCSC Ensembl
Outerchr16:14727039..15361518hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38634480
hg19634480
hg18634480
hg17634480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10946, nssv9523, nssv10945, nssv1295, nssv6660, nssv10079, nssv10080, nssv1294, nssv2134, nssv10078, nssv5588, nssv10947, nssv9522, nssv5587
SamplesNA18507, NA12156, NA18956, NA15510, NA18555, NA19240, NA19129
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)nsv7277
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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