A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6855



Internal ID15190323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88861932..90045325hg38UCSC Ensembl
Outerchr2:89161444..90084157hg19UCSC Ensembl
Outerchr2:88942559..89721462hg18UCSC Ensembl
Outerchr2:89000706..89779609hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381183394
hg19922714
hg18778904
hg17778904
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7318
Supporting Variants
SamplesNA12156
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)nssv6855
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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