A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357423



Internal ID22583092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35603625..35603779hg38UCSC Ensembl
chr11:35625173..35625327hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924463
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357423
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