A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508835



Internal ID20882139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92690239..92706793hg38UCSC Ensembl
chr15:93233469..93250023hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3816555
hg1916555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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