A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615755



Internal ID20988826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5567265..5604776hg38UCSC Ensembl
chr7:5606896..5644407hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3837512
hg1937512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230023
Samples
Known GenesFSCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615755
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