A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495258



Internal ID22553191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48434378..48449687hg38UCSC Ensembl
chr4:48436395..48451704hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3815310
hg1915310
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839051
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495258
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