A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4251



Internal ID15192292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9073081..9088772hg38UCSC Ensembl
Outerchr17:8976398..8992089hg19UCSC Ensembl
Outerchr17:8917123..8932814hg18UCSC Ensembl
Outerchr17:8917123..8932814hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3815692
hg1915692
hg1815692
hg1715692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7289
Supporting Variants
SamplesNA12878
Known GenesNTN1
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)nssv4251
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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