A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586862



Internal ID21535418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64551588..64552013hg38UCSC Ensembl
chr15:64843787..64844212hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096262
SamplesNA12878
Known GenesZNF609
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586862
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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