A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721634



Internal ID19019915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32179274..32382318hg38UCSC Ensembl
Innerchr15:32471475..32674519hg19UCSC Ensembl
Innerchr15:30258767..30461811hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38203045
hg19203045
hg18203045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042737
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)nssv3721634
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