A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506123



Internal ID20879399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47598318..47599263hg38UCSC Ensembl
chr15:47890515..47891460hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024245
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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