A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838637



Internal ID22613572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21104469..21108685hg38UCSC Ensembl
chr4:21106092..21110308hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg384217
hg194217
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1565n209
Supporting Variantsnssv17492805
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838637
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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