A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7102



Internal ID15190076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87929857..87971087hg38UCSC Ensembl
Outerchr4:88851009..88892239hg19UCSC Ensembl
Outerchr4:89070033..89111263hg18UCSC Ensembl
Outerchr4:89208188..89249418hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3841231
hg1941231
hg1841231
hg1741231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7364
Supporting Variants
SamplesNA12156
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)nssv7102
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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