A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870808



Internal ID22645744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6057128..6059445hg38UCSC Ensembl
chr17:5960448..5962765hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg382318
hg192318
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870808
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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