A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401853



Internal ID22459723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34678983..34685193hg38UCSC Ensembl
chr19:35169888..35176098hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg386211
hg196211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937911
Supporting Variants
Samples
Known GenesZNF302
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401853
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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