A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598938



Internal ID20972009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39301985..39302774hg38UCSC Ensembl
chr21:40673911..40674700hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254754
Samples
Known GenesBRWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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