A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343490



Internal ID21001043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218890287..218893008hg38UCSC Ensembl
chr2:219755009..219757730hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382722
hg192722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085490
Samples
Known GenesWNT10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343490
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