A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499448



Internal ID20872668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56889809..56893629hg38UCSC Ensembl
chr15:57182007..57185827hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025255
Samples
Known GenesLOC145783
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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