A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929403



Internal ID22704656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60548440..60548524hg38UCSC Ensembl
chr17:58625801..58625885hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929403
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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