A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555388



Internal ID20928478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56534280..56534773hg38UCSC Ensembl
chr3:56568308..56568801hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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