A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895083



Internal ID22670160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150463133..150467514hg38UCSC Ensembl
chr5:149842696..149847077hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg384382
hg194382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895083
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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