A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942200



Internal ID22717634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77717771..77718439hg38UCSC Ensembl
chr17:75713853..75714521hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942200
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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