A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827950



Internal ID22602885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12225380..12228107hg38UCSC Ensembl
chr1:12285437..12288164hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382728
hg192728
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv19n209
Supporting Variantsnssv17467453, nssv17455734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827950
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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