A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400764



Internal ID22458634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138925517..138926871hg38UCSC Ensembl
chr2:139683087..139684441hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400764
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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