A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352148



Internal ID21009701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206573633..206574287hg38UCSC Ensembl
chr2:207438357..207439011hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082970
Samples
Known GenesADAM23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352148
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