A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788653



Internal ID19170131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92629860..93065551hg38UCSC Ensembl
Innerchr13:93282113..93717804hg19UCSC Ensembl
Innerchr13:92080114..92515805hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38435692
hg19435692
hg18435692
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892425
Supporting Variants
Samples
Known GenesGPC5, GPC5-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=97
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788653
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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