A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905792



Internal ID22680984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76759733..76760800hg38UCSC Ensembl
chr5:76055558..76056625hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905792
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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