A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609064



Internal ID20982135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3084701..3167000hg38UCSC Ensembl
chr7:3124335..3206633hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3882300
hg1982299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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