A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606478



Internal ID20979549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10208124..10214512hg38UCSC Ensembl
chr7:10247751..10254139hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg386389
hg196389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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