A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515368



Internal ID291849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64539628..64543567hg38UCSC Ensembl
chr15:64831827..64835766hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383940
hg193940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704206
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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