A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901781



Internal ID22676934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99997428..99998158hg38UCSC Ensembl
chr4:100918585..100919315hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901781
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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