A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458648



Internal ID21116201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37810196..38520706hg38UCSC Ensembl
chr12:38203998..38914508hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38710511
hg19710511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187854
Samples
Known GenesALG10B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458648
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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