A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900297



Internal ID22675438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114006894..114006955hg38UCSC Ensembl
chr3:113725741..113725802hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402979
Samples
Known GenesKIAA1407
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900297
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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