A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502055



Internal ID20875296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48276150..48276782hg38UCSC Ensembl
chr15:48568347..48568979hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024726
Samples
Known GenesSLC12A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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