A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423227



Internal ID21080780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142329053..142452113hg38UCSC Ensembl
chr7:142179850..142276197hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38123061
hg1996348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7141n223
Supporting Variantsnssv18230379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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