A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472073



Internal ID21129626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7768134..7791427hg38UCSC Ensembl
chr12:7920730..7944023hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3823294
hg1923294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1361n223
Supporting Variantsnssv18180923
Samples
Known GenesNANOG, NANOGNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472073
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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