A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947099



Internal ID22722600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37471139..37485546hg38UCSC Ensembl
chr19:37962041..37976448hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3814408
hg1914408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395635
Samples
Known GenesZNF570
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947099
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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