A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182756



Internal ID20749796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38601518..38604533hg38UCSC Ensembl
chr17:36757771..36760786hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383016
hg193016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499917
Supporting Variants
Samples
Known GenesSRCIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182756
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