A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525612



Internal ID20898973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37259712..37260672hg38UCSC Ensembl
chr20:35888115..35889075hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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