A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7320



Internal ID15205632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:95395525..95686232hg38UCSC Ensembl
Outerchr2:96061273..96351980hg19UCSC Ensembl
Outerchr2:95425000..95715707hg18UCSC Ensembl
Outerchr2:95483147..95773854hg17UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38290708
hg19290708
hg18290708
hg17290708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11017, nssv10224
SamplesNA18956, NA15510
Known GenesFAHD2A, TRIM43, TRIM43B
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)nsv7320
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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