A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999271



Internal ID19158807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72284165..72343736hg38UCSC Ensembl
Innerchr1:72749848..72809419hg19UCSC Ensembl
Innerchr1:72522436..72582007hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3859572
hg1959572
hg1859572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv181n100
Supporting Variantsnssv3480013
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)nsv999271
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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