A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551952



Internal ID20925083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43713821..43714069hg38UCSC Ensembl
chr1:44179492..44179740hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251011
Samples
Known GenesST3GAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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