A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9320



Internal ID15193585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9073047..9102752hg38UCSC Ensembl
Outerchr17:8976364..9006069hg19UCSC Ensembl
Outerchr17:8917089..8946794hg18UCSC Ensembl
Outerchr17:8917089..8946794hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3829706
hg1929706
hg1829706
hg1729706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7289
Supporting Variants
SamplesNA18517
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)nssv9320
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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