A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497027



Internal ID20870230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38737901..38750000hg38UCSC Ensembl
chr15:39030102..39042201hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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