A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184577



Internal ID20751617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85959525..86146541hg38UCSC Ensembl
chr11:85670568..85857583hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38187017
hg19187016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473125
Supporting Variants
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184577
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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