A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970387



Internal ID22745322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43616308..43616308hg38UCSC Ensembl
chr19:44120460..44120460hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396599
Samples
Known GenesZNF428
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970387
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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