A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791314



Internal ID19165414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18469418..18995288hg38UCSC Ensembl
Innerchr13:19043558..19569428hg19UCSC Ensembl
Innerchr13:17941558..18467428hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38525871
hg19525871
hg18525871
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892294
Supporting Variants
Samples
Known GenesANKRD20A9P, LINC00408, LINC00417
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=77
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791314
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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