A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399077



Internal ID22456947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33747322..33747642hg38UCSC Ensembl
chr20:32335128..32335448hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948967
Supporting Variants
Samples
Known GenesZNF341
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399077
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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