A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618212



Internal ID20991283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66084902..66085804hg38UCSC Ensembl
chr7:65549889..65550791hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157975
Samples
Known GenesASL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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