A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905219



Internal ID22680403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163580788..163581100hg38UCSC Ensembl
chr4:164501940..164502252hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414068
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905219
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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