A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400482



Internal ID22458352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186118613..186178916hg38UCSC Ensembl
chr2:186983340..187043643hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3860304
hg1960304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400482
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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