A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2807961



Internal ID21253299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154378946..154379265hg38UCSC Ensembl
chr3:154096735..154097054hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709330
Samples
Known GenesGPR149
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2807961
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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