A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025836



Internal ID20592876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77205064..77363488hg38UCSC Ensembl
chr15:77497406..77655830hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38158425
hg19158425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508760
Supporting Variants
Samples
Known GenesLINC00597, PEAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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