A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522667



Internal ID20896028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30659874..30661916hg38UCSC Ensembl
chr19:31150781..31152823hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg382043
hg192043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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