A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598689



Internal ID21547317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2939024..2939093hg38UCSC Ensembl
chr19:2939022..2939091hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104370
SamplesHG00731
Known GenesZNF77
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598689
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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