A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9625



Internal ID15193492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13086336..13102158hg38UCSC Ensembl
Outerchr1:13153798..13169626hg19UCSC Ensembl
Outerchr1:13076385..13092213hg18UCSC Ensembl
Outerchr1:12977781..12993609hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3815823
hg1915829
hg1815829
hg1715829
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7172
Supporting Variants
SamplesNA18507
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)nssv9625
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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