A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469128



Internal ID21126681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91604275..91773853hg38UCSC Ensembl
chr12:91998052..92167630hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38169579
hg19169579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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