A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877714



Internal ID22652678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49894662..49896791hg38UCSC Ensembl
chr17:47972025..47974155hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg382130
hg192131
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877714
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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