A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527576



Internal ID303670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36256702..36266576hg38UCSC Ensembl
chr20:34844624..34854498hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389875
hg199875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732184
Samples
Known GenesAAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527576
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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