A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471333



Internal ID21128886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80707601..80709000hg38UCSC Ensembl
chr12:81101380..81102779hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003671
Samples
Known GenesMYF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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