A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705604



Internal ID21377880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11741546..11741871hg38UCSC Ensembl
chr2:11881672..11881997hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389570
Supporting Variants
Samples
Known GenesLPIN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705604
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.12931


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