A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929753



Internal ID22705011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5836343..5872474hg38UCSC Ensembl
chr17:5739663..5775794hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3836132
hg1936132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371252
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929753
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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