A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523602



Internal ID20896963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2526867..2530734hg38UCSC Ensembl
chr20:2507513..2511380hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383868
hg193868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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