A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv26n209



Internal ID22826101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15160405..15165038hg38UCSC Ensembl
chr1:15486901..15491534hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384634
hg194634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5875535, nsv5887500
Samples
Known GenesC1orf195, TMEM51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv26n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer