A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895602



Internal ID22670686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28364587..28375179hg38UCSC Ensembl
chr4:28366209..28376801hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3810593
hg1910593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895602
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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