A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878588



Internal ID22653554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16037298..16060502hg38UCSC Ensembl
chr1:16363793..16386997hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3823205
hg1923205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv27n209
Supporting Variantsnssv17350883
Samples
Known GenesCLCNKB, FAM131C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878588
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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