A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026438



Internal ID20593478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80781152..80785557hg38UCSC Ensembl
chr15:81073493..81077898hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384406
hg194406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500341
Supporting Variants
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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