A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025002



Internal ID20592043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47314301..47357200hg38UCSC Ensembl
chr15:47606498..47649397hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3842900
hg1942900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499225
Supporting Variants
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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