A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535600



Internal ID20908961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40003528..40014870hg38UCSC Ensembl
chr20:38632170..38643512hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3811343
hg1911343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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