A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947107



Internal ID22722609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2868486..2868791hg38UCSC Ensembl
chr19:2868484..2868789hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409047
Samples
Known GenesZNF556
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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