A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996946



Internal ID21906289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25329052..25329146hg38UCSC Ensembl
chr4:25330674..25330768hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538523
Samples
Known GenesZCCHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996946
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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