A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546968



Internal ID20920178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37980241..37980964hg38UCSC Ensembl
chr1:38445913..38446636hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252408
Samples
Known GenesSF3A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546968
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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