A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001928



Internal ID19091145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41317573..41782346hg38UCSC Ensembl
Innerchr3:41359064..41823838hg19UCSC Ensembl
Innerchr3:41334068..41798842hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38464774
hg19464775
hg18464775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4723n100
Supporting Variantsnssv3739706
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001928
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