A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506913



Internal ID20880201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76040401..76085500hg38UCSC Ensembl
chr15:76332742..76377841hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3845100
hg1945100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181319
Samples
Known GenesC15orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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