A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896148



Internal ID22671237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178929311..178934193hg38UCSC Ensembl
chr3:178647099..178651981hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384883
hg194883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896148
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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