A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510537



Internal ID20883857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39970701..39984700hg38UCSC Ensembl
chr15:40262902..40276901hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182507
Samples
Known GenesEIF2AK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510537
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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