A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472162



Internal ID22530054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60114845..60121944hg38UCSC Ensembl
chr16:60148749..60155848hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873989
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472162
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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