A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460979



Internal ID21118532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93804901..93808900hg38UCSC Ensembl
chr12:94198677..94202676hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1655n223
Supporting Variantsnssv18006241
Samples
Known GenesCRADD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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