A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900092



Internal ID22675231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173854695..173854878hg38UCSC Ensembl
chr4:174775846..174776029hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900092
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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