A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892976



Internal ID22668033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15898721..15903479hg38UCSC Ensembl
chr4:15900344..15905102hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg384759
hg194759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892976
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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