A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932544



Internal ID22707844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70613007..70613112hg38UCSC Ensembl
chr17:68609148..68609253hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932544
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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