A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596939



Internal ID20970010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39457655..39458633hg38UCSC Ensembl
chr21:40829581..40830559hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254767
Samples
Known GenesSH3BGR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596939
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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