A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901620



Internal ID22676772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27606040..27633259hg38UCSC Ensembl
chr5:27606147..27633366hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3827220
hg1927220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901620
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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