A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6436



Internal ID15190742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1880610..1919558hg38UCSC Ensembl
Outerchr11:1901840..1940788hg19UCSC Ensembl
Outerchr11:1858416..1897364hg18UCSC Ensembl
Outerchr11:1858416..1897364hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3838949
hg1938949
hg1838949
hg1738949
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7213
Supporting Variants
SamplesNA12156
Known GenesLSP1
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)nssv6436
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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