A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404532



Internal ID22462402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101314488..101323327hg38UCSC Ensembl
chr2:101930950..101939789hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg388840
hg198840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404532
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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