A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503898



Internal ID20877156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90773357..90774165hg38UCSC Ensembl
chr14:91239701..91240509hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022713
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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