A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904688



Internal ID22679866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55818953..55823186hg38UCSC Ensembl
chr4:56685119..56689352hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg384234
hg194234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425234
Samples
Known GenesLOC644145
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904688
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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