A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766064



Internal ID22100536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50906474..50906547hg38UCSC Ensembl
chr19:51409730..51409803hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440302
Supporting Variants
Samples
Known GenesKLK4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766064
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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