A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7198



Internal ID15205497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6148374..7383204hg38UCSC Ensembl
Outerchr10:6190337..7425166hg19UCSC Ensembl
Outerchr10:6230343..7465172hg18UCSC Ensembl
Outerchr10:6230343..7465172hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381234831
hg191234830
hg181234830
hg171234830
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11234
SamplesNA15510
Known GenesLINC00706, LINC00707, LOC399715, MIR3155A, MIR3155B, PFKFB3, PRKCQ, PRKCQ-AS1, SFMBT2
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)nsv7198
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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