A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495580



Internal ID21153133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122467562..122472387hg38UCSC Ensembl
chr12:122952109..122956934hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384826
hg194826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1718n223
Supporting Variantsnssv17998711
Samples
Known GenesZCCHC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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