A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026851



Internal ID20593891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80079493..80083173hg38UCSC Ensembl
chr15:80371835..80375515hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383681
hg193681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506841
Supporting Variants
Samples
Known GenesZFAND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026851
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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