A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563729



Internal ID20936800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35098792..35103926hg38UCSC Ensembl
chr4:35100414..35105548hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg385135
hg195135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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