A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088355



Internal ID21433611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27827891..27827949hg38UCSC Ensembl
chr16:27839212..27839270hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603815
Supporting Variants
SamplesHG00731
Known GenesGSG1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088355
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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