A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544878



Internal ID20918116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39309323..39309909hg38UCSC Ensembl
chr21:40681249..40681835hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072385
Samples
Known GenesBRWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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