A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2163



Internal ID15194760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9073074..9101950hg38UCSC Ensembl
Outerchr17:8976391..9005267hg19UCSC Ensembl
Outerchr17:8917116..8945992hg18UCSC Ensembl
Outerchr17:8917116..8945992hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3828877
hg1928877
hg1828877
hg1728877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7289
Supporting Variants
SamplesNA18555
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)nssv2163
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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