A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434580



Internal ID213251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126397314..126397483hg38UCSC Ensembl
chr3:126116157..126116326hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937624
Samples
Known GenesCCDC37
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434580
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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