A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031180



Internal ID19120401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85219177..85283386hg38UCSC Ensembl
Innerchr5:84514995..84579204hg19UCSC Ensembl
Innerchr5:84550751..84614960hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3864210
hg1964210
hg1864210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747338
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)nsv1031180
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