A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532404



Internal ID20905765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3930431..3935808hg38UCSC Ensembl
chr19:3930429..3935806hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385378
hg195378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047871
Samples
Known GenesNMRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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