A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004122



Internal ID21913465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113740820..113747788hg38UCSC Ensembl
chr7:113380875..113387843hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg386969
hg196969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004122
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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