A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342014



Internal ID20999567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134066711..134075912hg38UCSC Ensembl
chr2:134824282..134833483hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg389202
hg199202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342014
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