A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597059



Internal ID20970130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26075973..26077015hg38UCSC Ensembl
chr21:27448289..27449331hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4578n223
Supporting Variantsnssv18252964
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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