A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596963



Internal ID20970034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36931981..36932646hg38UCSC Ensembl
chr20:35560384..35561049hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254327
Samples
Known GenesSAMHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596963
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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