A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034566



Internal ID21943909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122482364..122482441hg38UCSC Ensembl
chr12:122966911..122966988hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599853
Samples
Known GenesZCCHC8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034566
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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