A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491887



Internal ID22549814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100885407..100887706hg38UCSC Ensembl
chr5:100221111..100223410hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840821
Supporting Variants
Samples
Known GenesST8SIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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