A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887585



Internal ID22662577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14873491..14873560hg38UCSC Ensembl
chr3:14914998..14915067hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416985
Samples
Known GenesFGD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887585
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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