A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507742



Internal ID20881037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62203601..62227400hg38UCSC Ensembl
chr15:62495800..62519599hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3823800
hg1923800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2562n223
Supporting Variantsnssv18189259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507742
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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