A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696437



Internal ID21218290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:220849..220938hg38UCSC Ensembl
chr17:70640..70729hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797094
Supporting Variants
Samples
Known GenesRPH3AL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696437
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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