A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10441



Internal ID15195671
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 StatusS
Merged Variantsnsv7369
Supporting Variants
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)nssv10441
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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