A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475338



Internal ID21132891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31812248..31814546hg38UCSC Ensembl
chr12:31965182..31967480hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg382299
hg192299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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