A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744530



Internal ID20520529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149480793..149481759hg38UCSC Ensembl
chr6:149801929..149802895hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290573
Samples
Known GenesZC3H12D
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744530
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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