A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749658



Internal ID20525690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46734424..46734484hg38UCSC Ensembl
chr6:46702161..46702221hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280112
Samples
Known GenesPLA2G7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749658
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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