A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2496



Internal ID15193943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13086337..13102010hg38UCSC Ensembl
Outerchr1:13153799..13169478hg19UCSC Ensembl
Outerchr1:13076386..13092065hg18UCSC Ensembl
Outerchr1:12977782..12993461hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3815674
hg1915680
hg1815680
hg1715680
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7172
Supporting Variants
SamplesNA18555
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)nssv2496
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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