A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420621



Internal ID21078174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129219222..129230124hg38UCSC Ensembl
chr7:128859063..128869965hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3810903
hg1910903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225766
Samples
Known GenesAHCYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420621
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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