A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436863



Internal ID215471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61407619..61413619hg38UCSC Ensembl
chr2:61634754..61640754hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16914897
Samples
Known GenesUSP34
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436863
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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