A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110554



Internal ID21451073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168863979..168864035hg38UCSC Ensembl
chr2:169720489..169720545hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572850
Supporting Variants
SamplesHG01505
Known GenesNOSTRIN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110554
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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