A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025137



Internal ID21934480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108237184..108238912hg38UCSC Ensembl
chr12:108630961..108632689hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381729
hg191729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610006
Samples
Known GenesWSCD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025137
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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