A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192056



Internal ID21330928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49621964..49621964hg38UCSC Ensembl
chr10:50830010..50830010hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949448
Supporting Variants
SamplesHG002
Known GenesCHAT
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192056
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer