A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830752



Internal ID22605687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75619743..75645253hg38UCSC Ensembl
chr1:76085428..76110938hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3825511
hg1925511
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830752
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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