A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181749



Internal ID20748789
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 StatusS
Merged Variantsnsv6501455
Supporting Variants
Samples
Known GenesBLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181749
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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