A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016231



Internal ID19105450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97870538..98084731hg38UCSC Ensembl
Innerchr5:97206242..97420435hg19UCSC Ensembl
Innerchr5:97231998..97446191hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38214194
hg19214194
hg18214194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640465
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)nsv1016231
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