A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612386



Internal ID20985457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87287883..87337489hg38UCSC Ensembl
chr7:86917199..86966805hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3849607
hg1949607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161208
Samples
Known GenesTP53TG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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