A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018384



Internal ID21927727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23565756..23592871hg38UCSC Ensembl
chr7:23605375..23632490hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3827116
hg1927116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563322
Samples
Known GenesCLK2P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018384
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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