A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542085



Internal ID20915351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35030058..35066149hg38UCSC Ensembl
chr21:36402355..36438446hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3836092
hg1936092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072125
Samples
Known GenesRUNX1, RUNX1-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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