A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501474



Internal ID20874708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1773474..1774462hg38UCSC Ensembl
chr17:1676768..1677756hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38989
hg19989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191338
Samples
Known GenesSERPINF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501474
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