A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7291



Internal ID15552286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:19013693..19236640hg38UCSC Ensembl
Outerchr17:18917006..19139953hg19UCSC Ensembl
Outerchr17:18857731..19080546hg18UCSC Ensembl
Outerchr17:18857731..19080546hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38222948
hg19222948
hg18222816
hg17222816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2166, nssv9542
SamplesNA18507, NA18555
Known GenesGRAP, GRAPL, SLC5A10
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)nsv7291
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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