A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557604



Internal ID20930675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148391318..148392487hg38UCSC Ensembl
chr3:148109105..148110274hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5052n223
Supporting Variantsnssv18262564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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