A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008432



Internal ID18750963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197054355..197093610hg38UCSC Ensembl
Innerchr3:196781226..196820481hg19UCSC Ensembl
Innerchr3:198265623..198304878hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3839256
hg1939256
hg1839256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5037n100
Supporting Variantsnssv3617004
Samples
Known GenesDLG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008432
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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