A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4433



Internal ID15192474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88827183..90179318hg38UCSC Ensembl
Outerchr2:89126696..90218159hg19UCSC Ensembl
Outerchr2:88907811..89855464hg18UCSC Ensembl
Outerchr2:88965958..89913611hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381352136
hg191091464
hg18947654
hg17947654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7318
Supporting Variants
SamplesNA12878
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)nssv4433
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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