A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408713



Internal ID22466583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15481512..15481610hg38UCSC Ensembl
chr2:15621636..15621734hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887020
Supporting Variants
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408713
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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