A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880694



Internal ID22655664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43118443..43120333hg38UCSC Ensembl
chr17:41270460..41272350hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381891
hg191891
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473822
Samples
Known GenesBRCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880694
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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