A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561537



Internal ID20934608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155242185..155242818hg38UCSC Ensembl
chr3:154959974..154960607hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561537
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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