A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477672



Internal ID22535573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23458984..23472200hg38UCSC Ensembl
chr16:23470305..23483521hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3813217
hg1913217
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883790
Supporting Variants
Samples
Known GenesGGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477672
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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