A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357470



Internal ID22583139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5480009..5480096hg38UCSC Ensembl
chr10:5521972..5522059hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357470
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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