A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485277



Internal ID22543188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31603952..31608751hg38UCSC Ensembl
chr20:30191755..30196554hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882866
Supporting Variants
Samples
Known GenesID1, MIR3193
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485277
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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