A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11015



Internal ID15193007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88868734..89134302hg38UCSC Ensembl
Outerchr2:89168246..89433785hg19UCSC Ensembl
Outerchr2:88949361..89214900hg18UCSC Ensembl
Outerchr2:89007508..89273047hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38265569
hg19265540
hg18265540
hg17265540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7318
Supporting Variants
SamplesNA15510
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)nssv11015
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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