A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459708



Internal ID21117261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95191869..95193396hg38UCSC Ensembl
chr12:95585645..95587172hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381528
hg191528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005857
Samples
Known GenesFGD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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