A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539709



Internal ID20913004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29379002..29379741hg38UCSC Ensembl
chr21:30751322..30752061hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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