A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552803



Internal ID20925930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17596401..17598200hg38UCSC Ensembl
chr21:18968719..18970518hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069443
Samples
Known GenesBTG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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