A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007234



Internal ID21916577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53335795..53532811hg38UCSC Ensembl
chr7:53403488..53600504hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38197017
hg19197017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007234
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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