A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325573



Internal ID20858704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159463696..160016249hg38UCSC Ensembl
chr1:159433486..159986039hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38552554
hg19552554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053530
Samples
Known GenesAPCS, C1orf204, CCDC19, CRP, DUSP23, FCRL6, IGSF9, LINC01133, OR10J5, SLAMF8, SLAMF9, TAGLN2, VSIG8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325573
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer