A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609792



Internal ID20982863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2864348..2864619hg38UCSC Ensembl
chr7:2903982..2904253hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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