A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4242



Internal ID15192283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:3109956..3232965hg38UCSC Ensembl
Outerchr17:3013250..3136259hg19UCSC Ensembl
Outerchr17:2960000..3083009hg18UCSC Ensembl
Outerchr17:2960000..3083009hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38123010
hg19123010
hg18123010
hg17123010
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7288
Supporting Variants
SamplesNA12878
Known GenesOR1A1, OR1A2, OR1G1
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)nssv4242
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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