A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438565



Internal ID21096118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68775801..68781400hg38UCSC Ensembl
chr9:71390717..71396316hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221206
Samples
Known GenesFAM122A, PIP5K1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438565
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