A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877399



Internal ID22652364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119380601..119380736hg38UCSC Ensembl
chr1:119923224..119923359hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364598
Samples
Known GenesHAO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877399
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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