A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553624



Internal ID20926735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40425720..40426208hg38UCSC Ensembl
chr3:40467211..40467699hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260622
Samples
Known GenesENTPD3, ENTPD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553624
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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