A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7379



Internal ID15552382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:35600020..35632305hg38UCSC Ensembl
Outerchr6:35567797..35600082hg19UCSC Ensembl
Outerchr6:35675775..35708060hg18UCSC Ensembl
Outerchr6:35675775..35708060hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3832286
hg1932286
hg1832286
hg1732286
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6061
SamplesNA12156
Known GenesFKBP5
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)nsv7379
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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