A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605318



Internal ID20978389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66969746..66986695hg38UCSC Ensembl
chr7:66434733..66451682hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3816950
hg1916950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605318
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer