A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11088



Internal ID15192934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87895884..87929971hg38UCSC Ensembl
Outerchr4:88817036..88851123hg19UCSC Ensembl
Outerchr4:89036060..89070147hg18UCSC Ensembl
Outerchr4:89174215..89208302hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3834088
hg1934088
hg1834088
hg1734088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7364
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)nssv11088
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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