A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501455



Internal ID20874688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90722345..90726504hg38UCSC Ensembl
chr15:91265576..91269735hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384160
hg194160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181749
Samples
Known GenesBLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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