A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828452



Internal ID22603387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:188024310..188070896hg38UCSC Ensembl
chr1:187993441..188040027hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3846587
hg1946587
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828452
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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