A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477774



Internal ID21135327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108760420..108767900hg38UCSC Ensembl
chr12:109154196..109161676hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg387481
hg197481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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