A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499740



Internal ID22557676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157700319..157720504hg38UCSC Ensembl
chr4:158621471..158641656hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3820186
hg1920186
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838372
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499740
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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