A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535628



Internal ID20908986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56665374..56665944hg38UCSC Ensembl
chr3:56699402..56699972hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261490
Samples
Known GenesFAM208A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535628
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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