A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426784



Internal ID21084337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128928557..128933609hg38UCSC Ensembl
chr7:128568611..128573663hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg385053
hg195053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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