A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499372



Internal ID20872591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88758867..88790264hg38UCSC Ensembl
chr14:89225211..89256608hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3831398
hg1931398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021611
Samples
Known GenesEML5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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