A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758196



Internal ID20534056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44490077..44490077hg38UCSC Ensembl
chr19:44994124..44994124hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261736
Samples
Known GenesZNF180
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758196
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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