A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426602



Internal ID22484472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141234565..141234893hg38UCSC Ensembl
chr4:142155719..142156047hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894173
Supporting Variants
Samples
Known GenesZNF330
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426602
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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