A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564872



Internal ID7035972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:177573081..177591248hg38UCSC Ensembl
Outerchr5:177000082..177018249hg19UCSC Ensembl
Outerchr5:176932688..176950855hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3818168
hg1918168
hg1818168
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010720
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564872
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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