A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871950



Internal ID22646888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48458983..48461192hg38UCSC Ensembl
chr19:48962240..48964449hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382210
hg192210
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477300
Samples
Known GenesKCNJ14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871950
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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