A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5727



Internal ID15197006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:10969806..11003191hg38UCSC Ensembl
Outerchr19:11080482..11113867hg19UCSC Ensembl
Outerchr19:10941482..10974867hg18UCSC Ensembl
Outerchr19:10941482..10974867hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3833386
hg1933386
hg1833386
hg1733386
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7305
Supporting Variants
SamplesNA19129
Known GenesSMARCA4
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)nssv5727
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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