A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177568



Internal ID21316364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15882463..15882581hg38UCSC Ensembl
chr19:15993273..15993391hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949789
Supporting Variants
SamplesHG002
Known GenesCYP4F2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177568
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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