A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616110



Internal ID20989181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11213517..11344928hg38UCSC Ensembl
chr7:11253144..11384555hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38131412
hg19131412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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