A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750772



Internal ID20526632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160077872..160077872hg38UCSC Ensembl
chr1:160047662..160047662hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750772
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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