A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349852



Internal ID21007405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99901853..99908444hg38UCSC Ensembl
chr2:100518315..100524906hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg386592
hg196592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090546
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349852
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