A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477569



Internal ID22535470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30060701..30071087hg38UCSC Ensembl
chr17:28387719..28398105hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3810387
hg1910387
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886777
Supporting Variants
Samples
Known GenesEFCAB5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477569
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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