A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477530



Internal ID22535431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28755346..28763013hg38UCSC Ensembl
chr17:27082364..27090031hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg387668
hg197668
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878910
Supporting Variants
Samples
Known GenesFAM222B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477530
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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