A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189614



Internal ID21328462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110411738..110411738hg38UCSC Ensembl
chr10:112171496..112171496hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945824
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189614
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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