A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473125



Internal ID21130678
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 StatusM
Merged Variants
Supporting Variantsnssv18184577
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473125
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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