A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023990



Internal ID21933333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64539519..64543473hg38UCSC Ensembl
chr15:64831718..64835672hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383955
hg193955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599113
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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