A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189565



Internal ID21328412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38087571..38087571hg38UCSC Ensembl
chr10:38376499..38376499hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3932820
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189565
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