A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617308



Internal ID20990379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116668932..116669485hg38UCSC Ensembl
chr6:116990095..116990648hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617308
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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