A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873449



Internal ID22648396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63297699..63298001hg38UCSC Ensembl
chr1:63763370..63763672hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370684
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873449
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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