A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733315



Internal ID156981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57892029..57896576hg38UCSC Ensembl
chr20:56467085..56471632hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg384548
hg194548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515670
Supporting Variants
Samples
Known GenesMIR4532
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733315
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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