A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009664



Internal ID21919007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:893149..893249hg38UCSC Ensembl
chr7:932786..932886hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565153
Samples
Known GenesGET4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009664
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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