A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7286



Internal ID15205594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75167099..75264317hg38UCSC Ensembl
Outerchr16:75200997..75298215hg19UCSC Ensembl
Outerchr16:73758498..73855716hg18UCSC Ensembl
Outerchr16:73758498..73855716hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3897219
hg1997219
hg1897219
hg1797219
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1322, nssv9318, nssv5615, nssv6679, nssv1323, nssv10961, nssv2150, nssv9533, nssv5614, nssv4227, nssv10100, nssv4226, nssv10099, nssv2149, nssv6680, nssv9534
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA18517, NA19240, NA19129
Known GenesBCAR1, CTRB1, CTRB2, ZFP1
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)nsv7286
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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