A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357760



Internal ID21015313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129831131..129832054hg38UCSC Ensembl
chr3:129549974..129550897hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093241
Samples
Known GenesTMCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357760
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