A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479128



Internal ID21136681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110855866..110862954hg38UCSC Ensembl
chr12:111293670..111300758hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg387089
hg197089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996948
Samples
Known GenesCCDC63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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