A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876024



Internal ID22650984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50827175..50830640hg38UCSC Ensembl
chr19:51330431..51333896hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg383466
hg193466
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477417
Samples
Known GenesKLK15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876024
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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