A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756121



Internal ID20531981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9491838..9491838hg38UCSC Ensembl
chr19:9602514..9602514hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296573
Samples
Known GenesZNF560
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756121
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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