A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9542



Internal ID15539772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:19013693..19126915hg38UCSC Ensembl
Outerchr17:18917006..19030228hg19UCSC Ensembl
Outerchr17:18857731..18970953hg18UCSC Ensembl
Outerchr17:18857731..18970953hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38113223
hg19113223
hg18113223
hg17113223
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7291
Supporting Variants
SamplesNA18507
Known GenesGRAP, 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)nssv9542
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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