A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493068



Internal ID22550996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111536602..111543130hg38UCSC Ensembl
chr5:110872300..110878828hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg386529
hg196529
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840662
Supporting Variants
Samples
Known GenesSTARD4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493068
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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