A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9349



Internal ID15193614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88835061..88876072hg38UCSC Ensembl
Outerchr2:89134574..89175588hg19UCSC Ensembl
Outerchr2:88915689..88956703hg18UCSC Ensembl
Outerchr2:88973836..89014850hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3841012
hg1941015
hg1841015
hg1741015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7318
Supporting Variants
SamplesNA18517
Known Genes
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)nssv9349
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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