A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911315



Internal ID22686529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17980482..17982419hg38UCSC Ensembl
chr8:17837991..17839928hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446611
Samples
Known GenesPCM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911315
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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