A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955314



Internal ID16957501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:11552827..11568726hg38UCSC Ensembl
Outerchr3:11594301..11610200hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3815900
hg1915900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001334
SamplesBILGI_BIOE
Known GenesATG7, VGLL4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955314
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