A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944865



Internal ID21364934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136352225..136352312hg38UCSC Ensembl
chr9:139246677..139246764hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199779
SamplesHG002
Known GenesGPSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944865
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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