A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929593



Internal ID22704849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77873029..77873090hg38UCSC Ensembl
chr17:75869111..75869172hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929593
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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