A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2166



Internal ID15541449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:19024049..19236640hg38UCSC Ensembl
Outerchr17:18927362..19139953hg19UCSC Ensembl
Outerchr17:18868087..19080546hg18UCSC Ensembl
Outerchr17:18868087..19080546hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38212592
hg19212592
hg18212460
hg17212460
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7291
Supporting Variants
SamplesNA18555
Known GenesGRAP, GRAPL
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)nssv2166
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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