A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545238



Internal ID20918471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17009621..17010089hg38UCSC Ensembl
chr21:18381940..18382408hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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