A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2506n223



Internal ID22805474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42550721..42558599hg38UCSC Ensembl
chr15:42842919..42850797hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg387879
hg197879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6498158, nsv6508983
Samples
Known GenesHAUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2506n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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