A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706939



Internal ID21379215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214547168..214547218hg38UCSC Ensembl
chr2:215411892..215411942hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390172
Supporting Variants
Samples
Known GenesVWC2L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706939
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.183908


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer