A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6558



Internal ID15537305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:47617789..47650113hg38UCSC Ensembl
Outerchr13:48191924..48224248hg19UCSC Ensembl
Outerchr13:47089925..47122249hg18UCSC Ensembl
Outerchr13:47089925..47122249hg17UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3832325
hg1932325
hg1832325
hg1732325
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7241
Supporting Variants
SamplesNA12156
Known Genes
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)nssv6558
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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