A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465642



Internal ID21123195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92908787..92909967hg38UCSC Ensembl
chr12:93302563..93303743hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005796
Samples
Known GenesEEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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