A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498025



Internal ID20871233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70848580..70849159hg38UCSC Ensembl
chr15:71140919..71141498hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182476
Samples
Known GenesLARP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498025
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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