A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730941



Internal ID20506857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123052733..123053070hg38UCSC Ensembl
chr6:123373878..123374215hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272236
Samples
Known GenesCLVS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730941
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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