A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513069



Internal ID20886409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40497935..40499657hg38UCSC Ensembl
chr15:40790134..40791856hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381723
hg191723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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