A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544322



Internal ID20917562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229559457..229560438hg38UCSC Ensembl
chr1:229695204..229696185hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38982
hg19982
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv549n223
Supporting Variantsnssv18250333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544322
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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