A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456887



Internal ID21114440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8209601..8216300hg38UCSC Ensembl
chr12:8362197..8368896hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1383n223
Supporting Variantsnssv18186681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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