A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344528



Internal ID21002081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241505072..241505957hg38UCSC Ensembl
chr2:242444487..242445372hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085152
Samples
Known GenesSTK25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344528
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