A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460699



Internal ID21118252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:99681139..99755536hg38UCSC Ensembl
chr12:100074917..100149314hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3874398
hg1974398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006688
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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