A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533444



Internal ID20906805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25047901..25075100hg38UCSC Ensembl
chr20:25028537..25055736hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3827200
hg1927200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067149
Samples
Known GenesACSS1, VSX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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