A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476488



Internal ID22534386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78957717..78980930hg38UCSC Ensembl
chr17:76953799..76977012hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3823214
hg1923214
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869946
Supporting Variants
Samples
Known GenesLGALS3BP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476488
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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