A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755283



Internal ID20531143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137117198..137117198hg38UCSC Ensembl
chr6:137438335..137438335hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755283
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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