A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038079



Internal ID20605119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78157427..78158115hg38UCSC Ensembl
chr17:76153508..76154196hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529614
Supporting Variants
Samples
Known GenesC17orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00175


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