A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940926



Internal ID21360995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128152012..128152120hg38UCSC Ensembl
chr7:127792064..127792172hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198670
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940926
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