A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745385



Internal ID20521393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55714954..55715017hg38UCSC Ensembl
chr12:56108738..56108801hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745385
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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