A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538218



Internal ID20911541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41710901..41714100hg38UCSC Ensembl
chr21:43131061..43134260hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071546
Samples
Known GenesLINC00479
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538218
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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