A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9369



Internal ID15193634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:40029153..40076357hg38UCSC Ensembl
Outerchr21:41401080..41448284hg19UCSC Ensembl
Outerchr21:40322950..40370154hg18UCSC Ensembl
Outerchr21:40322950..40370154hg17UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3847205
hg1947205
hg1847205
hg1747205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7346
Supporting Variants
SamplesNA18517
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)nssv9369
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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