A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009031



Internal ID19098249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:181188711..181228141hg38UCSC Ensembl
Innerchr1:181157847..181197277hg19UCSC Ensembl
Innerchr1:179424470..179463900hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3839431
hg1939431
hg1839431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502468
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)nsv1009031
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