A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10455



Internal ID15542343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:64473227..64515792hg38UCSC Ensembl
Outerchr5:63769054..63811619hg19UCSC Ensembl
Outerchr5:63804810..63847375hg18UCSC Ensembl
Outerchr5:63804810..63847375hg17UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3842566
hg1942566
hg1842566
hg1742566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7370
Supporting Variants
SamplesNA18956
Known GenesRGS7BP
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)nssv10455
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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