A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027333



Internal ID21936676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64551542..64551616hg38UCSC Ensembl
chr15:64843741..64843815hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611716
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027333
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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