A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607221



Internal ID20980292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79162139..79162612hg38UCSC Ensembl
chr7:78791455..78791928hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158985
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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