A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548773



Internal ID20921955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33268875..33272737hg38UCSC Ensembl
chr21:34641180..34645042hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383863
hg193863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071963
Samples
Known GenesIL10RB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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