A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399704



Internal ID22457574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36254444..36254517hg38UCSC Ensembl
chr20:34842366..34842439hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959195
Supporting Variants
Samples
Known GenesAAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399704
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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