A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188981



Internal ID20756021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73221065..73243700hg38UCSC Ensembl
chr17:71217204..71239839hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3822636
hg1922636
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519102
Supporting Variants
Samples
Known GenesC17orf80, FAM104A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188981
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