A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489973



Internal ID22547894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21696559..21705709hg38UCSC Ensembl
chr3:21738051..21747201hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg389151
hg199151
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836105
Supporting Variants
Samples
Known GenesZNF385D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489973
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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