A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv938e214



Internal ID22756832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132728764..132733672hg38UCSC Ensembl
chr3:132447608..132452516hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg384909
hg194909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3597831, esv3597829
SamplesHG03112
Known GenesNPHP3-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv938e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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