A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514631



Internal ID20887986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48725199..48726486hg38UCSC Ensembl
chr15:49017396..49018683hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381288
hg191288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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