A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768001



Internal ID20543861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175231391..175232798hg38UCSC Ensembl
chr1:175200527..175201934hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381408
hg191408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768001
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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