A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553775



Internal ID20926888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25567370..25567795hg38UCSC Ensembl
chr21:26939682..26940107hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071656
Samples
Known GenesMIR155HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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