A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499907



Internal ID20873132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90926066..90928246hg38UCSC Ensembl
chr15:91469296..91471476hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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