A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073566



Internal ID21982799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128097584..128097584hg38UCSC Ensembl
chr7:127737636..127737636hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073566
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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