A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430416



Internal ID21087969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125841121..126322494hg38UCSC Ensembl
chr7:125481175..125962548hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38481374
hg19481374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430416
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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