A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886771



Internal ID22661760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21101466..21113970hg38UCSC Ensembl
chr17:21004779..21017283hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3812505
hg1912505
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886771
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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