A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751729



Internal ID21385452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41657032..41657600hg38UCSC Ensembl
chr15:41949230..41949798hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432224
Supporting Variants
SamplesBTQ055
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751729
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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