A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028568



Internal ID21937911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66516635..66517860hg38UCSC Ensembl
chr15:66808973..66810198hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608432
Samples
Known GenesZWILCH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028568
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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