A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018697



Internal ID21928040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92339117..92339271hg38UCSC Ensembl
chr7:91968431..91968585hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577051
Samples
Known GenesANKIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018697
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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