A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464207



Internal ID21121760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93803649..93808914hg38UCSC Ensembl
chr12:94197425..94202690hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg385266
hg195266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1655n223
Supporting Variantsnssv18006238
Samples
Known GenesCRADD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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