A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597062



Internal ID20970133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26062585..26062781hg38UCSC Ensembl
chr21:27434901..27435097hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4577n223
Supporting Variantsnssv18252962
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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