A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4842



Internal ID15543058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:64472952..64514528hg38UCSC Ensembl
Outerchr5:63768779..63810355hg19UCSC Ensembl
Outerchr5:63804535..63846111hg18UCSC Ensembl
Outerchr5:63804535..63846111hg17UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3841577
hg1941577
hg1841577
hg1741577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7370
Supporting Variants
SamplesNA19129
Known GenesRGS7BP
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)nssv4842
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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