A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931439



Internal ID22706723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42532540..42532850hg38UCSC Ensembl
chr17:40684558..40684868hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931439
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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