A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7420



Internal ID15552428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:36361716..36399836hg38UCSC Ensembl
Outerchr9:36361713..36399833hg19UCSC Ensembl
Outerchr9:36351713..36389833hg18UCSC Ensembl
Outerchr9:36351713..36389833hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3838121
hg1938121
hg1838121
hg1738121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6271
SamplesNA12156
Known GenesRNF38
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)nsv7420
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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