A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606296



Internal ID20979367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25070613..25078437hg38UCSC Ensembl
chr7:25110232..25118056hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg387825
hg197825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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