A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619884



Internal ID20992955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147394729..147399120hg38UCSC Ensembl
chr6:147715865..147720256hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg384392
hg194392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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