A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015181



Internal ID19104398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2990019..3013846hg38UCSC Ensembl
Innerchr5:2990133..3013960hg19UCSC Ensembl
Innerchr5:3043133..3066960hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3823828
hg1923828
hg1823828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746156
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)nsv1015181
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