A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829106



Internal ID22604041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210954475..210955818hg38UCSC Ensembl
chr1:211127817..211129160hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381344
hg191344
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449678, nssv17463873
Samples
Known GenesKCNH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829106
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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