A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529777



Internal ID305783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14627093..14627199hg38UCSC Ensembl
chr21:15999414..15999520hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734067
Samples
Known GenesLOC388813
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529777
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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