A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529370



Internal ID20902731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7439901..7440600hg38UCSC Ensembl
chr20:7420548..7421247hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529370
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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