A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514107



Internal ID20887458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90834625..90837966hg38UCSC Ensembl
chr15:91377855..91381196hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383342
hg193342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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