A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829955



Internal ID22604890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248926786..248936665hg38UCSC Ensembl
chr1:249220985..249230864hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg389880
hg199880
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469192, nssv17456846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829955
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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