A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414373



Internal ID21071926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63440998..63442780hg38UCSC Ensembl
chr6:64150903..64152685hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381783
hg191783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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