A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478928



Internal ID22536830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75185496..75190057hg38UCSC Ensembl
chr17:73181591..73186152hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384562
hg194562
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868376
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478928
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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