A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10313



Internal ID15195799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:39989557..40032309hg38UCSC Ensembl
Outerchr21:41361484..41404236hg19UCSC Ensembl
Outerchr21:40283354..40326106hg18UCSC Ensembl
Outerchr21:40283354..40326106hg17UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3842753
hg1942753
hg1842753
hg1742753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7346
Supporting Variants
SamplesNA18956
Known GenesDSCAM
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)nssv10313
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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