A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952395



Internal ID17301269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:82663725..82745024hg38UCSC Ensembl
Outerchr17:80621601..80702900hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3881300
hg1981300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998828
SamplesBILGI_BIOE
Known GenesFN3K, FN3KRP, RAB40B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952395
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