A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352391



Internal ID22578060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62693073..62693073hg38UCSC Ensembl
chr10:64452833..64452833hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352391
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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