A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095621



Internal ID21430862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58710716..58710801hg38UCSC Ensembl
chr16:58744620..58744705hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593831
Supporting Variants
SamplesHG00731
Known GenesGOT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095621
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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