A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7384



Internal ID15552388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:114625787..115362294hg38UCSC Ensembl
Outerchr6:114946951..115683458hg19UCSC Ensembl
Outerchr6:115053644..115790151hg18UCSC Ensembl
Outerchr6:115053644..115790151hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38736508
hg19736508
hg18736508
hg17736508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6084
SamplesNA12156
Known Genes
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)nsv7384
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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