A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014089



Internal ID19103309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76855052..76866051hg38UCSC Ensembl
Innerchr4:77776205..77787204hg19UCSC Ensembl
Innerchr4:77995229..78006228hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3811000
hg1911000
hg1811000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633829
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014089
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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