A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025723



Internal ID20592763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75336345..75336514hg38UCSC Ensembl
chr15:75628686..75628855hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510345
Supporting Variants
Samples
Known GenesCOMMD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00524


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