A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546758



Internal ID20919968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238108032..238108950hg38UCSC Ensembl
chr1:238271332..238272250hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv564n223
Supporting Variantsnssv18251426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546758
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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