A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525620



Internal ID20898981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41715127..41720050hg38UCSC Ensembl
chr19:42219046..42223969hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046368
Samples
Known GenesCEACAM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525620
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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