A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522279



Internal ID20895640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77451883..77567012hg38UCSC Ensembl
chr17:75447965..75563094hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38115130
hg19115130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187717
Samples
Known GenesLOC100507351, SEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522279
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