A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687449



Internal ID18639044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46620127..47343541hg38UCSC Ensembl
Innerchr8:47531749..48256108hg19UCSC Ensembl
Innerchr8:47650914..48418661hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38723415
hg19724360
hg18767748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028036
Supporting Variants
Samples
Known GenesLINC00293, LOC100287846, SPIDR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3687449
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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