A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718096



Internal ID19016377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79567321..79710708hg38UCSC Ensembl
Innerchr15:79859663..80003050hg19UCSC Ensembl
Innerchr15:77646718..77790105hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38143388
hg19143388
hg18143388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047966
Supporting Variants
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)nssv3718096
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