A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403668



Internal ID22461538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36464765..36464841hg38UCSC Ensembl
chr20:35093168..35093244hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961214
Supporting Variants
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403668
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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