A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757561



Internal ID20533421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25346740..25346740hg38UCSC Ensembl
chr12:25499674..25499674hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757561
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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