A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431382



Internal ID21088935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142457411..142494451hg38UCSC Ensembl
chr7:142137495..142174550hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3837041
hg1937056
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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