A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025623



Internal ID21934966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93190860..93195257hg38UCSC Ensembl
chr12:93584636..93589033hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg384398
hg194398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604141
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025623
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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