A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935410



Internal ID21355479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53671695..53671882hg38UCSC Ensembl
chr2:53898832..53899019hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178293
SamplesHG002
Known GenesASB3, GPR75-ASB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935410
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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