A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10664



Internal ID15542134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62816148..62860878hg38UCSC Ensembl
Outerchr9:66471972..66516702hg19UCSC Ensembl
Outerchr9:66211792..66256522hg18UCSC Ensembl
Outerchr9:64153244..64197974hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3844731
hg1944731
hg1844731
hg1744731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7425
Supporting Variants
SamplesNA18956
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)nssv10664
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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