A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529927



Internal ID20903288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3776085..3778319hg38UCSC Ensembl
chr19:3776083..3778317hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382235
hg192235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046674
Samples
Known GenesMATK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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