A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732875



Internal ID20508801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13392585..13398685hg38UCSC Ensembl
chr12:13545519..13551619hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv21n199
Supporting Variantsnssv16268887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732875
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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