A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892425



Internal ID19183245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92706621..93065551hg38UCSC Ensembl
Outerchr13:92629860..93065551hg38UCSC Ensembl
Innerchr13:93358874..93717804hg19UCSC Ensembl
Outerchr13:93282113..93717804hg19UCSC Ensembl
Innerchr13:92156875..92515805hg18UCSC Ensembl
Outerchr13:92080114..92515805hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38435692
hg19435692
hg18435692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788653, essv25789141
Samples
Known GenesGPC5, GPC5-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892425
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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