A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950534



Internal ID16952721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:107786279..107941478hg38UCSC Ensembl
Outerchr1:108328901..108484100hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38155200
hg19155200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997188
SamplesBILGI_BIOE
Known GenesMIR7852, VAV3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950534
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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