A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101885



Internal ID21428660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63361017..63361017hg38UCSC Ensembl
chr18:61028250..61028250hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645042
Supporting Variants
SamplesHG00731
Known GenesKDSR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101885
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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