A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929818



Internal ID22705077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5781744..5781957hg38UCSC Ensembl
chr17:5685064..5685277hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381015
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929818
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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