A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420341



Internal ID21077894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142392405..142797003hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38404599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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