A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746712



Internal ID20522726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34018849..34018915hg38UCSC Ensembl
chr15:34311050..34311116hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265101
Samples
Known GenesAVEN, CHRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746712
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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