A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829672



Internal ID22604607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26912532..26913531hg38UCSC Ensembl
chr1:27239023..27240022hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468642
Samples
Known GenesNR0B2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829672
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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