A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9368



Internal ID15540319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:34613044..34644134hg38UCSC Ensembl
Outerchr21:35985343..36016433hg19UCSC Ensembl
Outerchr21:34907213..34938303hg18UCSC Ensembl
Outerchr21:34907213..34938303hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3831091
hg1931091
hg1831091
hg1731091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7345
Supporting Variants
SamplesNA18517
Known GenesRCAN1
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)nssv9368
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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