A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845499



Internal ID22620434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39308075..39317021hg38UCSC Ensembl
chr6:39275851..39284797hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg388947
hg198947
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505745
Samples
Known GenesKCNK16, KCNK17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845499
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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