A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638793



Internal ID21830840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35498275..35498275hg38UCSC Ensembl
chr21:36870573..36870573hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg384508
hg194508
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111874
Supporting Variants
Samples
Known GenesLOC100506403
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638793
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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