A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067559



Internal ID21976792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129077023..129077023hg38UCSC Ensembl
chr7:128717077..128717077hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067559
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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