A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515036



Internal ID20888392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34094429..34106369hg38UCSC Ensembl
chr15:34386630..34398570hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811941
hg1911941
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189496
Samples
Known GenesEMC7, PGBD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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