A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999258



Internal ID19158794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103674490..103717100hg38UCSC Ensembl
Innerchr3:103393334..103435944hg19UCSC Ensembl
Innerchr3:104876024..104918634hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3842611
hg1942611
hg1842611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604380
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)nsv999258
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