A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417521



Internal ID22475391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21696572..21705278hg38UCSC Ensembl
chr3:21738064..21746770hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388707
hg198707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891005
Supporting Variants
Samples
Known GenesZNF385D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417521
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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