A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549633



Internal ID20922795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21358263..21359271hg38UCSC Ensembl
chr21:22730583..22731591hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071317
Samples
Known GenesNCAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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