A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6623



Internal ID15537240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23205476..23215907hg38UCSC Ensembl
Outerchr15:22657161..22667592hg19UCSC Ensembl
Outerchr15:20208525..20218956hg18UCSC Ensembl
Outerchr15:20208525..20218956hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3810432
hg1910432
hg1810432
hg1710432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
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)nssv6623
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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