A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477420



Internal ID22535321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50940216..50950613hg38UCSC Ensembl
chr19:51443472..51453869hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3810398
hg1910398
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872771
Supporting Variants
Samples
Known GenesKLK5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477420
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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