A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503195



Internal ID20876447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95680956..95689157hg38UCSC Ensembl
chr14:96147293..96155494hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg388202
hg198202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022215
Samples
Known GenesTCL1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer