A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1790779



Internal ID12953897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45133340..45134491hg38UCSC Ensembl
chr17:43210707..43211858hg19UCSC Ensembl
chr17:40566233..40567384hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381152
hg191152
hg181152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3810321
SamplesHuRef
Known GenesACBD4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1790779
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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