A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879559



Internal ID22654529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7866225..7867666hg38UCSC Ensembl
chr17:7769543..7770984hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879559
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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