A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11168



Internal ID15192725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13082187..13106969hg38UCSC Ensembl
Outerchr1:13149650..13174441hg19UCSC Ensembl
Outerchr1:13072237..13097028hg18UCSC Ensembl
Outerchr1:12973633..12998424hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3824783
hg1924792
hg1824792
hg1724792
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7172
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)nssv11168
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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