A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054626



Internal ID19143845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72519061..72575161hg38UCSC Ensembl
Innerchr15:72811402..72867502hg19UCSC Ensembl
Innerchr15:70598456..70654556hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3856101
hg1956101
hg1856101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553694
Samples
Known GenesARIH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054626
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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