A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869770



Internal ID22644705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36488801..36515655hg38UCSC Ensembl
chr19:36979703..37006557hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3826855
hg1926855
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475292
Samples
Known GenesLOC728752, ZNF260, ZNF566
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869770
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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