A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736279



Internal ID20512226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2939040..2939111hg38UCSC Ensembl
chr19:2939038..2939109hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271609
Samples
Known GenesZNF77
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736279
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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