A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529307



Internal ID20902668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6017158..6021176hg38UCSC Ensembl
chr19:6017169..6021187hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384019
hg194019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049945
Samples
Known GenesLOC100128568, RFX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529307
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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