A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950987



Internal ID21371057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40561980..40561980hg38UCSC Ensembl
chr15:40854179..40854179hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381818
hg191818
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194591
SamplesHG002
Known GenesC15orf57
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950987
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