A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469887



Internal ID22527777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27709762..27713490hg38UCSC Ensembl
chr16:27721083..27724811hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383729
hg193729
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873554
Supporting Variants
Samples
Known GenesKIAA0556
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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