A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090740



Internal ID21462508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8178508..8180501hg38UCSC Ensembl
chr16:8228510..8230503hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381994
hg191994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604033
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090740
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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