A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361118



Internal ID21018671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52090701..52095300hg38UCSC Ensembl
chr3:52124717..52129316hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100956
Samples
Known GenesPOC1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361118
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