A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529769



Internal ID20903130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2945816..2952426hg38UCSC Ensembl
chr19:2945814..2952424hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386611
hg196611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3420n223
Supporting Variantsnssv18047471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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