A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184546



Internal ID20751586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98923575..99006958hg38UCSC Ensembl
chr12:99317353..99400736hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3883384
hg1983384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459084
Supporting Variants
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184546
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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