A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738378



Internal ID20514346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105171727..105172790hg38UCSC Ensembl
chr6:105619602..105620665hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295257
Samples
Known GenesPOPDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738378
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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