A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531336



Internal ID307298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64603889..64605061hg38UCSC Ensembl
chr15:64896088..64897260hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704213
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531336
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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