A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093432



Internal ID20660472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125290172..125290876hg38UCSC Ensembl
chr3:125009016..125009720hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356899
Supporting Variants
Samples
Known GenesZNF148
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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