A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10405



Internal ID15542393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49254197..49312723hg38UCSC Ensembl
Outerchr4:49256214..49314740hg19UCSC Ensembl
Outerchr4:48950971..49009497hg18UCSC Ensembl
Outerchr4:49097142..49155668hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3858527
hg1958527
hg1858527
hg1758527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7360
Supporting Variants
SamplesNA18956
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)nssv10405
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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