A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878416



Internal ID22653381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21345189..21400665hg38UCSC Ensembl
chr17:21248501..21303977hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3855477
hg1955477
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476238
Samples
Known GenesKCNJ12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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