A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545978



Internal ID20919198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34882601..34888600hg38UCSC Ensembl
chr21:36254898..36260897hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203928
Samples
Known GenesRUNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545978
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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