A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9640



Internal ID15540163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49251111..49322871hg38UCSC Ensembl
Outerchr4:49253128..49324888hg19UCSC Ensembl
Outerchr4:48947885..49019645hg18UCSC Ensembl
Outerchr4:49094056..49165816hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3871761
hg1971761
hg1871761
hg1771761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7360
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)nssv9640
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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