A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466965



Internal ID21124518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:99772836..99802383hg38UCSC Ensembl
chr12:100166614..100196161hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3829548
hg1929548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006703
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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