A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870724



Internal ID22645660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68119251..68127092hg38UCSC Ensembl
chr17:66115392..66123233hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg387842
hg197842
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475845
Samples
Known GenesLINC00674
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870724
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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