A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503197



Internal ID20876449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24992501..24993600hg38UCSC Ensembl
chr15:25237648..25238747hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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