A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953239



Internal ID17302113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:103828757..103830456hg38UCSC Ensembl
Outerchr3:103547601..103549300hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001436
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953239
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