A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570578



Internal ID20943649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185217268..185218060hg38UCSC Ensembl
chr3:184935056..184935848hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260601
Samples
Known GenesEHHADH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570578
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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