A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375183



Internal ID21032736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125297419..125297753hg38UCSC Ensembl
chr3:125016263..125016597hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093434
Samples
Known GenesZNF148
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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