A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542078



Internal ID20915344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41599455..41712113hg38UCSC Ensembl
chr21:43019615..43132273hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38112659
hg19112659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203978
Samples
Known GenesLINC00111, LINC00479
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542078
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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