A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526893



Internal ID20900254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5960716..5966822hg38UCSC Ensembl
chr19:5960727..5966833hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386107
hg196107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049941
Samples
Known GenesRANBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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