A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7341



Internal ID15205655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:36795559..36809921hg38UCSC Ensembl
Outerchr20:35423962..35438324hg19UCSC Ensembl
Outerchr20:34857376..34871738hg18UCSC Ensembl
Outerchr20:34857376..34871738hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3814363
hg1914363
hg1814363
hg1714363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6941
SamplesNA12156
Known GenesSOGA1
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)nsv7341
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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