A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394004



Internal ID22451874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176992765..177014787hg38UCSC Ensembl
chr2:177857493..177879515hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3822023
hg1922023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897913
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394004
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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