A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459317



Internal ID21116870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93315029..93318337hg38UCSC Ensembl
chr12:93708805..93712113hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383309
hg193309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005811
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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