A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017462



Internal ID21926805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129290630..129296823hg38UCSC Ensembl
chr7:128930471..128936664hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg386194
hg196194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574076
Samples
Known GenesAHCYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017462
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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