A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517666



Internal ID20891027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41462316..41549519hg38UCSC Ensembl
chr19:41968222..42055887hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3887204
hg1987666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048085
Samples
Known GenesLOC100505495
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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