A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542552



Internal ID20915810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46278958..46289711hg38UCSC Ensembl
chr21:47698872..47709625hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810754
hg1910754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073086
Samples
Known GenesMCM3AP, YBEY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542552
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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