A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628811



Internal ID21820858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34684163..34684214hg38UCSC Ensembl
chr19:35175068..35175119hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044460
Supporting Variants
Samples
Known GenesZNF302
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628811
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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