A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755148



Internal ID20531008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9221380..9221380hg38UCSC Ensembl
chr12:9373976..9373976hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755148
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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