A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099180



Internal ID21475384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21289978..21290049hg38UCSC Ensembl
chr16:21301299..21301370hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603470
Supporting Variants
SamplesHG03371
Known GenesCRYM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099180
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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