A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653884



Internal ID21602189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50959670..50959670hg38UCSC Ensembl
chr19:51462926..51462926hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105673
SamplesHG00731
Known GenesKLK6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653884
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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