A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938245



Internal ID22713624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44693128..44694024hg38UCSC Ensembl
chr17:42770496..42771392hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938245
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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