A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552624



Internal ID20925749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:154598485..154599185hg38UCSC Ensembl
chr2:155454997..155455697hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552624
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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