A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549765



Internal ID20922920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60963137..61303044hg38UCSC Ensembl
chr3:60948809..61288718hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38339908
hg19339910
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262211
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549765
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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