A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7369



Internal ID15205685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:18907517..26650615hg38UCSC Ensembl
Outerchr5:18907626..26650724hg19UCSC Ensembl
Outerchr5:18943383..26686481hg18UCSC Ensembl
Outerchr5:18943383..26686481hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg387743099
hg197743099
hg187743099
hg177743099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10441
SamplesNA18956
Known GenesCDH10, CDH12, CDH18, GUSBP1, LOC340107, PMCHL1, PRDM9
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)nsv7369
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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