A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177397



Internal ID21316193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50331239..50331296hg38UCSC Ensembl
chr19:50834496..50834553hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954255
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177397
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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