A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882626



Internal ID22657603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42174728..42175727hg38UCSC Ensembl
chr17:40326746..40327745hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473786
Samples
Known GenesKCNH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882626
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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