A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502656



Internal ID20875902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38045054..38045818hg38UCSC Ensembl
chr15:38337255..38338019hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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