A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183825



Internal ID21322621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36511607..36511673hg38UCSC Ensembl
chr14:36980812..36980878hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953999
Supporting Variants
SamplesHG002
Known GenesSFTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183825
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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