A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929752



Internal ID22705010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34018831..34018896hg38UCSC Ensembl
chr15:34311032..34311097hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382504
Samples
Known GenesAVEN, CHRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929752
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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