A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353158



Internal ID22578827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70151259..70151259hg38UCSC Ensembl
chr10:71911015..71911015hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962587
Supporting Variants
Samples
Known GenesSAR1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353158
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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