A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027178



Internal ID19116397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:82132207..82193269hg38UCSC Ensembl
Innerchr5:81428026..81489088hg19UCSC Ensembl
Innerchr5:81463782..81524844hg18UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3861063
hg1961063
hg1861063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639137
Samples
Known GenesATG10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027178
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer