A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv257n172



Internal ID22814631
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 StatusM
Merged Variants
Supporting Variantsnsv4432224, nsv4432225
SamplesBTQ038, BTQ055, BTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv257n172
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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