A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6275



Internal ID15537588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62814226..62862884hg38UCSC Ensembl
Outerchr9:66470050..66518708hg19UCSC Ensembl
Outerchr9:66209870..66258528hg18UCSC Ensembl
Outerchr9:64151322..64199980hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3848659
hg1948659
hg1848659
hg1748659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7425
Supporting Variants
SamplesNA12156
Known GenesPTGER4P2-CDK2AP2P2
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)nssv6275
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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