A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503997



Internal ID20877255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95660084..95678334hg38UCSC Ensembl
chr14:96126421..96144671hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3818251
hg1918251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022214
Samples
Known GenesTCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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