A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261416



Internal ID20828456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52944598..52945671hg38UCSC Ensembl
chr3:52978614..52979687hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg381074
hg191074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551241
Supporting Variants
Samples
Known GenesSFMBT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261416
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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