A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487231



Internal ID21144784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109046875..109051371hg38UCSC Ensembl
chr12:109484680..109489176hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg384497
hg194497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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