A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737039



Internal ID20512995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48014641..48014730hg38UCSC Ensembl
chr12:48408424..48408513hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737039
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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