A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026729



Internal ID20593769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85776325..85783440hg38UCSC Ensembl
chr15:86319556..86326671hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg387116
hg197116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505360
Supporting Variants
Samples
Known GenesKLHL25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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