A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013549



Internal ID19102767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72743357..72942690hg38UCSC Ensembl
Innerchr1:73209040..73408373hg19UCSC Ensembl
Innerchr1:72981628..73180961hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38199334
hg19199334
hg18199334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3475594
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)nsv1013549
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