A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499663



Internal ID22557599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147573854..147580378hg38UCSC Ensembl
chr4:148495006..148501530hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg386525
hg196525
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499663
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