A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024771



Internal ID21934114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64190018..64190084hg38UCSC Ensembl
chr15:64482217..64482283hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609516
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024771
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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