A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833676



Internal ID22608611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61808441..61820553hg38UCSC Ensembl
chr2:62035576..62047688hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3812113
hg1912113
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1147n209
Supporting Variantsnssv17487556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833676
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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