A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183665



Internal ID21322461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23925343..23925396hg38UCSC Ensembl
chr14:24394552..24394605hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942614
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183665
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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