A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029617



Internal ID19118835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86364309..86469705hg38UCSC Ensembl
Innerchr5:85660127..85765522hg19UCSC Ensembl
Innerchr5:85695883..85801278hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38105397
hg19105396
hg18105396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639182
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)nsv1029617
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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