A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456292



Internal ID21113845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32469447..32480667hg38UCSC Ensembl
chr12:32622381..32633601hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3811221
hg1911221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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