A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885837



Internal ID22660823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19273136..19287717hg38UCSC Ensembl
chr1:19599630..19614211hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3814582
hg1914582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360446
Samples
Known GenesAKR7A3, AKR7L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885837
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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