A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025418



Internal ID19114636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84853619..84906954hg38UCSC Ensembl
Innerchr5:84149437..84202772hg19UCSC Ensembl
Innerchr5:84185193..84238528hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3853336
hg1953336
hg1853336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5712n100
Supporting Variantsnssv3747336, nssv3639170
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)nsv1025418
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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