A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998256



Internal ID19157793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104363103..104560543hg38UCSC Ensembl
Innerchr3:104081947..104279387hg19UCSC Ensembl
Innerchr3:105564637..105762077hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38197441
hg19197441
hg18197441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4832n100
Supporting Variantsnssv3604384
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)nsv998256
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