A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv259n172



Internal ID22814633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61228513..61229410hg38UCSC Ensembl
chr15:61520712..61521609hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4432239, nsv4432240
SamplesBTQ016, SMI018, NB09
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv259n172
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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