A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10545



Internal ID15542253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:54237198..54341047hg38UCSC Ensembl
Outerchr7:54304891..54408740hg19UCSC Ensembl
Outerchr7:54272385..54376234hg18UCSC Ensembl
Outerchr7:54079100..54182949hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38103850
hg19103850
hg18103850
hg17103850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7397
Supporting Variants
SamplesNA18956
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)nssv10545
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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