A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529303



Internal ID20902664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5750738..5757367hg38UCSC Ensembl
chr20:5731384..5738013hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg386630
hg196630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069078
Samples
Known GenesC20orf196
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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