A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512825



Internal ID20886164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31361096..31403773hg38UCSC Ensembl
chr17:29688114..29730791hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3842678
hg1942678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191040
Samples
Known GenesNF1, RAB11FIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512825
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