A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490613



Internal ID22548537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27671736..27677207hg38UCSC Ensembl
chr3:27713227..27718698hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg385472
hg195472
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490613
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