A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200529



Internal ID20767569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155604647..155742765hg38UCSC Ensembl
chr1:155574438..155712556hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38138119
hg19138119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334322
Supporting Variants
Samples
Known GenesDAP3, MSTO1, MSTO2P, YY1AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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