A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215586



Internal ID20782626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132766392..132781641hg38UCSC Ensembl
chr6:133087531..133102780hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3815250
hg1915250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600447
Supporting Variants
Samples
Known GenesSLC18B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215586
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