A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357506



Internal ID22583175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115664462..115665016hg38UCSC Ensembl
chr11:115535180..115535734hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357506
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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