A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224907



Internal ID20791947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136769701..136803200hg38UCSC Ensembl
chr9:139664153..139697652hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3833500
hg1933500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450226
Supporting Variants
Samples
Known GenesCCDC183, TMEM141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224907
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