A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875775



Internal ID22650733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33769763..33794418hg38UCSC Ensembl
chr20:32357569..32382224hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3824656
hg1924656
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485310
Samples
Known GenesZNF341
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875775
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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