A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616888



Internal ID20989959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10778266..10828342hg38UCSC Ensembl
chr7:10817893..10867969hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3850077
hg1950077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616888
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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