A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465782



Internal ID21123335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8208901..8228600hg38UCSC Ensembl
chr12:8361497..8381196hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3819700
hg1919700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1385n223
Supporting Variantsnssv18196194
Samples
Known GenesFAM90A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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