A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875973



Internal ID22650933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35280475..35283710hg38UCSC Ensembl
chr17:33607494..33610729hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383236
hg193236
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875973
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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