A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6080



Internal ID15191098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13086932..13100760hg38UCSC Ensembl
Outerchr1:13154394..13168236hg19UCSC Ensembl
Outerchr1:13076981..13090823hg18UCSC Ensembl
Outerchr1:12978377..12992219hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3813829
hg1913843
hg1813843
hg1713843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7172
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)nssv6080
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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