A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039013



Internal ID21948356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64371907..64372027hg38UCSC Ensembl
chr15:64664106..64664226hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614872
Samples
Known GenesKIAA0101
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039013
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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