A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596012



Internal ID20969083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39199926..39200727hg38UCSC Ensembl
chr21:40571852..40572653hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254749
Samples
Known GenesBRWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596012
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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