A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735112



Internal ID20511052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87507518..87507736hg38UCSC Ensembl
chr12:87901295..87901513hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735112
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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