A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504786



Internal ID20878049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41957924..41964344hg38UCSC Ensembl
chr15:42250122..42256542hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386421
hg196421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023916
Samples
Known GenesEHD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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