A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013499



Internal ID19102717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208905758..208953571hg38UCSC Ensembl
Innerchr1:209079103..209126916hg19UCSC Ensembl
Innerchr1:207145726..207193539hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3847814
hg1947814
hg1847814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv568n100
Supporting Variantsnssv3494113
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)nsv1013499
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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