A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398083



Internal ID22455953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65804349..65809089hg38UCSC Ensembl
chr2:66031483..66036223hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg384741
hg194741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398083
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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