A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008831



Internal ID19098049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:167118276..167136547hg38UCSC Ensembl
Innerchr1:167087513..167105784hg19UCSC Ensembl
Innerchr1:165354137..165372408hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3818272
hg1918272
hg1818272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502282
Samples
Known GenesDUSP27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008831
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