A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744268



Internal ID20520266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4247575..4247639hg38UCSC Ensembl
chr19:4247572..4247636hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277502
Samples
Known GenesCCDC94
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744268
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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