A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407833



Internal ID22465703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61153375..61153375hg38UCSC Ensembl
chr20:59728431..59728431hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407833
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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