A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024723



Internal ID20591763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48248848..48251955hg38UCSC Ensembl
chr15:48541045..48544152hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383108
hg193108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512726
Supporting Variants
Samples
Known GenesSLC12A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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