A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607545



Internal ID20980616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13650748..13707034hg38UCSC Ensembl
chr7:13690373..13746659hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3856287
hg1956287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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