A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003613



Internal ID6715742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:152261602..152304356hg38UCSC Ensembl
Outerchr1:152234078..152276832hg19UCSC Ensembl
Outerchr1:150500702..150543456hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3842755
hg1942755
hg1842755
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563823
SamplesHuRef
Known GenesFLG
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003613
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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