A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191652



Internal ID21330513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62928909..62928909hg38UCSC Ensembl
chr10:64688669..64688669hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937060
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191652
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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