A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839179



Internal ID22614114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21104468..21107873hg38UCSC Ensembl
chr4:21106091..21109496hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg383406
hg193406
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1565n209
Supporting Variantsnssv17492804
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839179
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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