A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551025



Internal ID20924165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35614131..35651314hg38UCSC Ensembl
chr21:36986429..37023612hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3837184
hg1937184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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