A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183335



Internal ID21322131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61755315..61755365hg38UCSC Ensembl
chr14:62222033..62222083hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935555
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183335
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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