A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476023



Internal ID21133576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110849861..110850174hg38UCSC Ensembl
chr12:111287665..111287978hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996947
Samples
Known GenesCCDC63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476023
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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