A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941959



Internal ID22717390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73278854..73278944hg38UCSC Ensembl
chr17:71274993..71275083hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941959
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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