A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9645



Internal ID15193472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87888542..87935477hg38UCSC Ensembl
Outerchr4:88809694..88856629hg19UCSC Ensembl
Outerchr4:89028718..89075653hg18UCSC Ensembl
Outerchr4:89166873..89213808hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3846936
hg1946936
hg1846936
hg1746936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7364
Supporting Variants
SamplesNA18507
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)nssv9645
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer