A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895463



Internal ID22670546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56045444..56046372hg38UCSC Ensembl
chr5:55341271..55342199hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426278
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895463
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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