A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180923



Internal ID20747963
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 StatusS
Merged Variantsnsv6472073
Supporting Variants
Samples
Known GenesNANOG, NANOGNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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