A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832677



Internal ID22607612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44809549..44811704hg38UCSC Ensembl
chr2:45036688..45038843hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg382156
hg192156
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486104, nssv17485567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832677
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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