A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489022



Internal ID21146575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39535801..39538200hg38UCSC Ensembl
chr14:40005005..40007404hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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